CPC Probe
FDA 510(k) K961380 · Carl Zeiss, Inc.
510(k) numberK961380
Submission
- Device name
- CPC Probe
- Applicant
- Carl Zeiss, Inc.
Thornwood, NY, US - Received
- April 10, 1996
- Decision date
- March 17, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary 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
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|---|---|---|---|
| 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 |
|---|---|---|
| K013402 | Visulas 532SGEX · Special | 11/14/2001SE |
| K003885 | Visulas Yag IIGEX · Traditional | 02/22/2001SE |
| K993357 | IolmasterHJO · Traditional | 03/20/2000SE |
| K983868 | Opmi Twiner Surgical MicroscopeGEX · Traditional | 01/29/1999SE |
| K965139 | Surgical Microscope Navigator (SMN) System/Surgical Tool Navigator (STN) SystemHAW · Traditional | 04/23/1997SE |
| K961171 | Humphrey Oct ScannerHLI · Traditional | 06/21/1996SE |
| K954167 | Humphrey Field Analyzer (Hfa II)HPT · Traditional | 11/24/1995SE |
| K952894 | Visulink 900 ArgonHQF · Traditional | 08/14/1995SE |
| K950985 | Zeiss Endolive Stero EndoscopeGCJ · Traditional | 03/29/1995SE |
| K931478 | Zeiss Opmi L Stereo-LaparoscopeHET · Traditional | 09/28/1994SE |
Questions and answers
When was CPC Probe cleared by the FDA?
CPC Probe (K961380) received a 510(k) decision of Substantially Equivalent on March 17, 1997, 341 days after the submission was received.
What is the product code of K961380?
The FDA product code is GEX – Powered Laser Surgical Instrument, a Class II (moderate risk) device regulated under 21 CFR 878.4810.