AST/SGOT— 510(k) K965126
Substantially EquivalentDerma Media Lab., Inc.
FDA 510(k) clearance K965126 for AST/SGOT, Substantially Equivalent on 1997-01-17. Applicant: Derma Media Lab., Inc.. Device class: 2.
Clearance details
- Applicant
- Derma Media Lab., Inc.
- Product code
- Code CIT
- Device class
- Class 2
- Regulation
- 21 CFR 862.1100
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Fe Springs, CA, US
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More clearances from Derma Media Lab., Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.