The following data is part of a premarket notification filed by Dermascalp Llc with the FDA for Dermascalp Laser Cap.
Device ID | K152587 |
510k Number | K152587 |
Device Name: | DermaScalp Laser Cap |
Classification | Laser, Comb, Hair |
Applicant | DERMASCALP LLC 1700 ALMA DR SUITE 400 Plano, TX 75075 |
Contact | John Carullo |
Correspondent | John Carullo DERMASCALP LLC 1700 ALMA DR SUITE 400 Plano, TX 75075 |
Product Code | OAP |
CFR Regulation Number | 890.5500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-10 |
Decision Date | 2016-02-04 |
Summary: | summary |