RIA-GNOST FERRITIN— 510(k) K890697

Name: FDA 510(k) clearance K890697
Creator: U.S. Food and Drug Administration
Published: 1989-03-16

Substantially Equivalent

Cambridge Medical Technology

FDA 510(k) clearance K890697 for RIA-GNOST FERRITIN, Substantially Equivalent on 1989-03-16. Applicant: Cambridge Medical Technology. Device class: 2.

Clearance details

Applicant: Cambridge Medical Technology
Product code: Code JMG
Device class: Class 2
Regulation: 21 CFR 866.5340
Advisory panel: Immunology
Date received: 1989-02-10
Decision date: 1989-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Billerica, MA, US

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