TWIN-FUSOR/UNI-FUSOR BLOOD & FLUID INFUSION CUFF— 510(k) K893519

Name: FDA 510(k) clearance K893519
Creator: U.S. Food and Drug Administration
Published: 1989-08-15

Substantially Equivalent

Statlabs, Inc.

FDA 510(k) clearance K893519 for TWIN-FUSOR/UNI-FUSOR BLOOD & FLUID INFUSION CUFF, Substantially Equivalent on 1989-08-15. Applicant: Statlabs, Inc.. Device class: 1.

Clearance details

Applicant: Statlabs, Inc.
Product code: Code KZB
Device class: Class 1
Regulation: 21 CFR 866.2170
Advisory panel: Microbiology
Date received: 1989-05-08
Decision date: 1989-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin, TN, US

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