FIBRINOGEN UPTAKE SYS -VARIOUS MODELS— 510(k) K834168

Name: FDA 510(k) clearance K834168
Creator: U.S. Food and Drug Administration
Published: 1983-12-29

Substantially Equivalent

Canberra Industries, Inc.

FDA 510(k) clearance K834168 for FIBRINOGEN UPTAKE SYS -VARIOUS MODELS, Substantially Equivalent on 1983-12-29. Applicant: Canberra Industries, Inc.. Device class: 1.

Clearance details

Applicant: Canberra Industries, Inc.
Product code: Code JZD
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1983-11-04
Decision date: 1983-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Meriden, CT, US

Download summary PDF View on FDA.gov ↗

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