FISHER DIAGNOSTICS LATEST-CRP TEST KIT— 510(k) K850160
Substantially EquivalentFisher Diagnostics
FDA 510(k) clearance K850160 for FISHER DIAGNOSTICS LATEST-CRP TEST KIT, Substantially Equivalent on 1985-04-19. Applicant: Fisher Diagnostics. Device class: 2.
Clearance details
- Applicant
- Fisher Diagnostics
- Product code
- Code DCK
- Device class
- Class 2
- Regulation
- 21 CFR 866.5270
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Orangeburg, NY, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.