Laserscope Omniplus Photosurgical SYSTEM/CO2 Laser
FDA 510(k) K862005 · Laserscope
510(k) numberK862005
Submission
- Device name
- Laserscope Omniplus Photosurgical SYSTEM/CO2 Laser
- Applicant
- Laserscope
Santa Clara, CA, US - Received
- May 27, 1986
- Decision date
- August 29, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- EWG – Laser, Ent Microsurgical Carbon-Dioxide
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.4500
- Specialty
- Ear, Nose, Throat
Other 510(k)s with product code EWG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K924652 | Benson CCA100EWG · Traditional | Benson Medical Instruments Co. | 04/09/1993SE |
| K870587 | Lasermatic Surgilaser Model 5050EWG · Traditional | Lasermatic OY | 08/10/1988SN |
| K880429 | Illumina 55 CO2 Laser SystemEWG · Traditional | Cooper Lasersonics, Inc. | 04/18/1988SE |
| K880428 | Illumina 25 CO2 Laser SystemEWG · Traditional | Cooper Lasersonics, Inc. | 04/18/1988SE |
| K880427 | Illumina 40 CO2 Laser SystemEWG · Traditional | Cooper Lasersonics, Inc. | 04/18/1988SE |
| K872710 | Model 20-B W/OB-10A/U Attach. for Ear, Nose/ThroatEWG · Traditional | Directed Energy, Inc. | 09/24/1987SE |
| K870840 | Model 20-C W/BR-20A/U Attach/Model HL-3.O AttachEWG · Traditional | Directed Energy, Inc. | 06/12/1987SE |
| K864975 | Laserscope Omniplus Photosurgical System for (ENT)EWG · Traditional | Laserscope | 02/25/1987SE |
| K862866 | Model 10-C W/LP-10A/U & OS-10A/U for Oral/Ent UseEWG · Traditional | Directed Energy, Inc. | 01/09/1987SE |
| K862865 | Model 10-C W/LP-10A/U & OB-10A/U for Oral/Ent UseEWG · Traditional | Directed Energy, Inc. | 01/09/1987SE |
More from Directed Energy, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K062719 | Greenlight HPS Series Surgical Laser System & AccessoriesGEX · Traditional | 12/01/2006SE |
| K061646 | Laserscope Guided Delivery Device (GDD) Cystourethroscope & AccessoriesFBO · Traditional | 06/27/2006SE |
| K034011 | Gemini Surgical Laser System & AccessoriesGEX · Traditional | 03/30/2004SE |
| K024206 | Aura Isurgical Laser System & AccessoriesGEX · Traditional | 11/17/2003SE |
| K020021 | Lyra Surgical Laser System and Accessiories (Nd:Yag Configuration)GEX · Traditional | 07/02/2002SE |
| K010834 | Lyra Series Surgical Laser System & AccessoriesGEX · Traditional | 05/21/2001SE |
| K010284 | Lyra G Series Surgical Laser System (SL Series Q-Switched Nd:Yag Configuration)GEX · Traditional | 05/01/2001SE |
| K003765 | Lyra G Series Surgical Laser System (SL Series Q-Switched Nd:Yag Configuration)GEX · Traditional | 03/06/2001SE |
| K003147 | Lyra Series Surgical Laser System (SL Series, Nd:Yag Configuration)GEX · Traditional | 12/15/2000SE |
| K990718 | Orion Series Surgical Laser System (SL Seriesq-Switched Nd:Yag Configuration)GEX · Traditional | 03/08/2000SE |
Questions and answers
When was Laserscope Omniplus Photosurgical SYSTEM/CO2 Laser cleared by the FDA?
Laserscope Omniplus Photosurgical SYSTEM/CO2 Laser (K862005) received a 510(k) decision of Substantially Equivalent on August 29, 1986, 94 days after the submission was received.
What is the product code of K862005?
The FDA product code is EWG – Laser, Ent Microsurgical Carbon-Dioxide, a Class II (moderate risk) device regulated under 21 CFR 874.4500.