The following data is part of a premarket notification filed by Palomar Medical Technologies, Inc. with the FDA for Abc Hair Removal System.
Device ID | K060839 |
510k Number | K060839 |
Device Name: | ABC HAIR REMOVAL SYSTEM |
Classification | Light Based Over-the-counter Hair Removal |
Applicant | PALOMAR MEDICAL TECHNOLOGIES, INC. 82 CAMBRIDGE ST. Burlington, MA 01803 |
Contact | Sharon Timberlake |
Correspondent | Sharon Timberlake PALOMAR MEDICAL TECHNOLOGIES, INC. 82 CAMBRIDGE ST. Burlington, MA 01803 |
Product Code | OHT |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-03-28 |
Decision Date | 2006-12-07 |
Summary: | summary |