BLOOD LINE COMP. NEG. PRESS. PILLOW— 510(k) K772355

Name: FDA 510(k) clearance K772355
Creator: U.S. Food and Drug Administration
Published: 1978-01-26

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K772355 for BLOOD LINE COMP. NEG. PRESS. PILLOW, Substantially Equivalent on 1978-01-26. Applicant: Cordis Corp.. Device class: 2.

Clearance details

Applicant: Cordis Corp.
Product code: Code FIW
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1977-12-27
Decision date: 1978-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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