The following data is part of a premarket notification filed by Palomar Medical Technologies, Inc. with the FDA for Palomar Q-yag 5 Nd:yag Laser System.
| Device ID | K061436 |
| 510k Number | K061436 |
| Device Name: | PALOMAR Q-YAG 5 ND:YAG LASER SYSTEM |
| Classification | Powered Laser Surgical Instrument |
| Applicant | PALOMAR MEDICAL TECHNOLOGIES, INC. 82 CAMBRIDGE ST. Burlington, MA 01803 |
| Contact | Sharon L Timberlake |
| Correspondent | Sharon L Timberlake PALOMAR MEDICAL TECHNOLOGIES, INC. 82 CAMBRIDGE ST. Burlington, MA 01803 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-05-24 |
| Decision Date | 2006-12-06 |
| Summary: | summary |