← Back to catalogue

Pulsaderm Acne Mask 28 , Pulsaderm Acne Mask 37

FDA 510(k)

Class II (US FDA 510(k))

510(k) K170111

by Pulsaderm Llc

Identifiers

510(k) Number
K170111 FDA 510(k)
FDA Product Code
OLP FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 878.4810 FDA 510(k)
Regulation Number
878.4810 FDA 510(k)
Advisory Committee
General, Plastic Surgery FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Pulsaderm Acne Mask 28 , Pulsaderm Acne Mask 37 by Pulsaderm Llc — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pulsaderm Llc
FDA Applicant
Pulsaderm, LLC

Sources (1)

  • FDA 510(k) K170111 24 fields · synced Jun 18, 2026