ANGIOMED HIGH PRESSURE CONNECTORS— 510(k) K863446

Name: FDA 510(k) clearance K863446
Creator: U.S. Food and Drug Administration
Published: 1986-09-23

Substantially Equivalent

Angiomed U.S., Inc.

FDA 510(k) clearance K863446 for ANGIOMED HIGH PRESSURE CONNECTORS, Substantially Equivalent on 1986-09-23. Applicant: Angiomed U.S., Inc.. Device class: 1.

Clearance details

Applicant: Angiomed U.S., Inc.
Product code: Code GCD
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1986-09-08
Decision date: 1986-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

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K760382 — CONNECTORS1976-11-02

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K864225 — ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT1987-01-30
K863386 — VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS1986-10-24
K862805 — ANGIOMED VAC-U-CUT BIOPSY NEEDLE1986-09-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.