U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL— 510(k) K870737
Substantially EquivalentU. S. Diagnostics, Inc.
FDA 510(k) clearance K870737 for U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL, Substantially Equivalent on 1987-04-13. Applicant: U. S. Diagnostics, Inc.. Device class: 1.
Clearance details
- Applicant
- U. S. Diagnostics, Inc.
- Product code
- Code JJT
- Device class
- Class 1
- Regulation
- 21 CFR 862.1660
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Luis Obispo, CA, US
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