N-ASSAY L AST/GOT— 510(k) K980902
Substantially EquivalentCrestat Diagnostics, Inc.
FDA 510(k) clearance K980902 for N-ASSAY L AST/GOT, Substantially Equivalent on 1998-03-26. Applicant: Crestat Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Crestat Diagnostics, 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
- Seattle, WA, US
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More clearances from Crestat Diagnostics, Inc.
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