DIGICAP— 510(k) K012199
Substantially EquivalentHumana USA, Inc.
FDA 510(k) clearance K012199 for DIGICAP, Substantially Equivalent on 2001-12-19. Applicant: Humana USA, Inc.. Device class: 1.
Clearance details
- Applicant
- Humana USA, Inc.
- Product code
- Code GAB
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bethesda, MD, US
Recent devices under product code GAB
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