KELOCATE SHEETING— 510(k) K982051
Substantially EquivalentAllied Biomedical Corp.
FDA 510(k) clearance K982051 for KELOCATE SHEETING, Substantially Equivalent on 1998-08-05. Applicant: Allied Biomedical Corp.. Device class: 1.
Clearance details
- Applicant
- Allied Biomedical Corp.
- Product code
- Code MDA
- Device class
- Class 1
- Regulation
- 21 CFR 878.4025
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paso Robles, CA, US
Recent devices under product code MDA
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