Model 130-SAS Aspirating Endophotocoagulator Laser
FDA 510(k) K944623 · Mnlase, Inc.
510(k) numberK944623
Submission
- Device name
- Model 130-SAS Aspirating Endophotocoagulator Laser
- Applicant
- Mnlase, Inc.
Reston, VA, US - Received
- September 20, 1994
- Decision date
- November 1, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- GEX – Powered Laser Surgical Instrument
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4810
- Specialty
- General, Plastic Surgery
A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue, for general surgical purpose in medical specialties of general and plastic surgery, dermatology/aesthetic, podiatry, otolaryngology (ent), gynecology…
Other 510(k)s with product code GEX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262426 | Medical Diode Laser (S1Pro+, S1Pro K15, S1Pro N6, S1Pro N75)GEX · Traditional | Wuhan Pioon Technology Co., Ltd. | 09/10/2026SE |
| K261562 | Diode Laser Therapy SystemGEX · Traditional | Sanhe LEFIS Electronics Co., Ltd. | 09/10/2026SE |
| K261589 | 1927nm Thulium Laser System (PZ-DJG85-01, PZ-DJG85-02)GEX · Traditional | Zhengzhou PZ Laser Slim Technology Co., Ltd. | 09/02/2026SE |
| K262269 | CO2 Laser System (MBT- CO2 Laser)GEX · Traditional | Beijing Mega Beauty Technology Co., Ltd. | 09/01/2026SE |
| K261821 | 1565nm Laser Therapy Device (PZ-JG86-01,PZ-JG86-02)GEX · Traditional | Zhengzhou PZ Laser Slim Technology Co., Ltd. | 08/27/2026SE |
| K262070 | Diode Laser Therapy Systems (DL612A)GEX · Traditional | Hebei Zollvan Medical Technology Co., Ltd. | 08/19/2026SE |
| K261964 | Echolaser X4GEX · Traditional | Elesta S.P.A | 08/19/2026SE |
| K261841 | Q Switched Nd:YAG Laser machine (QLQW-01)GEX · Traditional | Beijing Nubway S&T Co., Ltd. | 08/11/2026SE |
| K261221 | SOLTIVE Laser System (SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed…GEX · Traditional | Olympus Surgical Technologies America | 07/24/2026SE |
| K261738 | Medical Thulium Fiber Laser Systems (UroFiber 150Q)GEX · Traditional | Rhein Laser Technologies Co., Ltd. | 07/21/2026SE |
More from Rhein Laser Technologies Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K944630 | Model 230-SAS Laser Delivery ProbeGEX · Traditional | 11/09/1994SE |
| K944629 | Model 230-SAC Laser Delivery ProbeGEX · Traditional | 11/03/1994SE |
| K944628 | Model 220-SS Laser Delivery ProbeGEX · Traditional | 11/03/1994SE |
| K944627 | Model 220-SC Curved Endophotocoagulator LaserGEX · Traditional | 11/03/1994SE |
| K944626 | Model 210-AS Aspirating Endophotocoagulator LaserGEX · Traditional | 11/03/1994SE |
| K944625 | Model 210-AC Aspirating Endophotocoagulator LaserGEX · Traditional | 11/03/1994SE |
| K944471 | Straight Endophotocoagulator Laser ProbeGEX · Traditional | 11/03/1994SE |
| K944470 | Curved Endophotocoagulator Laser ProbeGEX · Traditional | 11/03/1994SE |
| K944632 | Model 120-SS Laser Delivery ProbeGEX · Traditional | 11/01/1994SE |
| K944631 | Model 120-SC Laser Delivery ProbeGEX · Traditional | 11/01/1994SE |
Questions and answers
When was Model 130-SAS Aspirating Endophotocoagulator Laser cleared by the FDA?
Model 130-SAS Aspirating Endophotocoagulator Laser (K944623) received a 510(k) decision of Substantially Equivalent on November 1, 1994, 42 days after the submission was received.
What is the product code of K944623?
The FDA product code is GEX – Powered Laser Surgical Instrument, a Class II (moderate risk) device regulated under 21 CFR 878.4810.