ANGIO MED DISPOSABLE PRESSURE CONNECTORS— 510(k) K855078

Name: FDA 510(k) clearance K855078
Creator: U.S. Food and Drug Administration
Published: 1986-02-19

Substantially Equivalent

Angiomed U.S., Inc.

FDA 510(k) clearance K855078 for ANGIO MED DISPOSABLE PRESSURE CONNECTORS, Substantially Equivalent on 1986-02-19. Applicant: Angiomed U.S., Inc.. Device class: 1.

Clearance details

Applicant: Angiomed U.S., Inc.
Product code: Code KGZ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1985-12-19
Decision date: 1986-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

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