FISHER DIAGNOSTICS LATEST-CRP TEST KIT— 510(k) K850160

Substantially Equivalent

Fisher Diagnostics

FDA 510(k) clearance K850160 for FISHER DIAGNOSTICS LATEST-CRP TEST KIT, Substantially Equivalent on 1985-04-19. Applicant: Fisher Diagnostics.

Clearance details

Applicant
Fisher Diagnostics
Product code
Code DCK
Advisory panel
Immunology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Orangeburg, NY, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.