DMS-1000C DERMOABRADER— 510(k) K963204
Substantially EquivalentAesthetic Lasers, Inc.
FDA 510(k) clearance K963204 for DMS-1000C DERMOABRADER, Substantially Equivalent on 1996-12-09. Applicant: Aesthetic Lasers, Inc.. Device class: 1.
Clearance details
- Applicant
- Aesthetic Lasers, Inc.
- Product code
- Code GFE
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Annapolis, MD, US
Recent devices under product code GFE
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