DermaScalp Laser Cap
K-Number: K173846 · 2018-03-21
Device Summary
Frequently Asked Questions
What is the DermaScalp Laser Cap?
DermaScalp Laser Cap is a medical device that received FDA 510(k) clearance on 2018-03-21. The listed applicant is Dermascalp, LLC. The 510(k) number is K173846.
When did DermaScalp Laser Cap receive FDA 510(k) clearance?
DermaScalp Laser Cap received FDA 510(k) clearance on 2018-03-21, under 510(k) number K173846.
Who is the listed applicant for DermaScalp Laser Cap?
The FDA 510(k) record lists Dermascalp, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DermaScalp Laser Cap?
The FDA product code for DermaScalp Laser Cap is OAP.
Other records listing Dermascalp, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OAP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.