THYROGLOBULIN AUTOANTIBODY ENZYME IMMUNOASSAY— 510(k) K936010
Substantially EquivalentBiomerica, Inc.
FDA 510(k) clearance K936010 for THYROGLOBULIN AUTOANTIBODY ENZYME IMMUNOASSAY, Substantially Equivalent on 1994-07-18. Applicant: Biomerica, Inc.. Device class: 2.
Clearance details
- Applicant
- Biomerica, Inc.
- Product code
- Code DDC
- Device class
- Class 2
- Regulation
- 21 CFR 866.5870
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newport Beach, CA, US
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More clearances from Biomerica, Inc.
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