The following data is part of a premarket notification filed by New Star Lasers, Inc. with the FDA for Cooltouch Model Ct3pz, Cooltouch Ct3 Plus Coolbreeze.
Device ID | K101783 |
510k Number | K101783 |
Device Name: | COOLTOUCH MODEL CT3PZ, COOLTOUCH CT3 PLUS COOLBREEZE |
Classification | Powered Laser Surgical Instrument |
Applicant | NEW STAR LASERS, INC. 9085 FOOTHILLS BLVD. Roseville, CA 95747 |
Contact | Natalie R Vollrath |
Correspondent | Natalie R Vollrath NEW STAR LASERS, INC. 9085 FOOTHILLS BLVD. Roseville, CA 95747 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-06-25 |
Decision Date | 2010-09-13 |
Summary: | summary |