CREATININE REAGENT— 510(k) K955938
Substantially EquivalentDerma Media Lab., Inc.
FDA 510(k) clearance K955938 for CREATININE REAGENT, Substantially Equivalent on 1996-03-12. Applicant: Derma Media Lab., Inc.. Device class: 2.
Clearance details
- Applicant
- Derma Media Lab., Inc.
- Product code
- Code CGX
- Device class
- Class 2
- Regulation
- 21 CFR 862.1225
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Fe Springs, CA, US
Recent devices under product code CGX
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