The following data is part of a premarket notification filed by Coherent Medical Group with the FDA for Coherent Versapulse Aesthetic Surgical Lasers.
| Device ID | K960032 |
| 510k Number | K960032 |
| Device Name: | COHERENT VERSAPULSE AESTHETIC SURGICAL LASERS |
| Classification | Powered Laser Surgical Instrument |
| Applicant | COHERENT MEDICAL GROUP 3270 W. BAYSHORE RD. P.O. BOX 10122 Palo Alto, CA 94303 |
| Contact | Anne Worden |
| Correspondent | Anne Worden COHERENT MEDICAL GROUP 3270 W. BAYSHORE RD. P.O. BOX 10122 Palo Alto, CA 94303 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-02 |
| Decision Date | 1996-04-01 |
| Summary: | summary |