VASCULAR ACCESS SYSTEM— 510(k) K810114

Name: FDA 510(k) clearance K810114
Creator: U.S. Food and Drug Administration
Published: 1981-03-26

Substantially Equivalent

Bentley Laboratories, Inc.

FDA 510(k) clearance K810114 for VASCULAR ACCESS SYSTEM, Substantially Equivalent on 1981-03-26. Applicant: Bentley Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Bentley Laboratories, Inc.
Product code: Code FIQ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1980-12-15
Decision date: 1981-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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