The following data is part of a premarket notification filed by Palomar Medical Products, Inc. with the FDA for Palomar Aspire Laser Platform.
| Device ID | K083165 |
| 510k Number | K083165 |
| Device Name: | PALOMAR ASPIRE LASER PLATFORM |
| Classification | Powered Laser Surgical Instrument |
| Applicant | PALOMAR MEDICAL PRODUCTS, INC. 82 CAMBRIDGE ST. Burlington, MA 01803 |
| Contact | Sharon Timberlake |
| Correspondent | Sharon Timberlake PALOMAR MEDICAL PRODUCTS, 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 | 2008-10-27 |
| Decision Date | 2009-02-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00841494100490 | K083165 | 000 |
| 00841494100483 | K083165 | 000 |
| 10841494100473 | K083165 | 000 |