RELIEF— 510(k) K812567
Substantially EquivalentAmerican Pharmaceutical Co., Inc.
FDA 510(k) clearance K812567 for RELIEF, Substantially Equivalent on 1981-11-10. Applicant: American Pharmaceutical Co., Inc.. Device class: Unclassified.
Clearance details
- Applicant
- American Pharmaceutical Co., Inc.
- Product code
- Code LKX
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code LKX
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