The following data is part of a premarket notification filed by Palomar Medical Technologies, Inc. with the FDA for Palomar Luxir Handpiece.
Device ID | K050370 |
510k Number | K050370 |
Device Name: | PALOMAR LUXIR HANDPIECE |
Classification | Lamp, Infrared, Therapeutic Heating |
Applicant | PALOMAR MEDICAL TECHNOLOGIES, INC. 131 KELEKENT LN. Cary, NC 27511 |
Contact | Marcy Moore |
Correspondent | Marcy Moore PALOMAR MEDICAL TECHNOLOGIES, INC. 131 KELEKENT LN. Cary, NC 27511 |
Product Code | ILY |
CFR Regulation Number | 890.5500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-02-14 |
Decision Date | 2005-06-15 |
Summary: | summary |