EVRON GEL— 510(k) K961222
Substantially EquivalentPharmaceutical Innovations, Inc.
FDA 510(k) clearance K961222 for EVRON GEL, Substantially Equivalent on 1996-06-26. Applicant: Pharmaceutical Innovations, Inc.. Device class: 1.
Clearance details
- Applicant
- Pharmaceutical Innovations, Inc.
- Product code
- Code KMJ
- Device class
- Class 1
- Regulation
- 21 CFR 880.6375
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code KMJ
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