DIAGNOSTIC INTRAVASCULAR CATHETER— 510(k) K930758

Name: FDA 510(k) clearance K930758
Creator: U.S. Food and Drug Administration
Published: 1993-09-24

Substantially Equivalent

Applied Medical Resources

FDA 510(k) clearance K930758 for DIAGNOSTIC INTRAVASCULAR CATHETER, Substantially Equivalent on 1993-09-24. Applicant: Applied Medical Resources. Device class: 2.

Clearance details

Applicant: Applied Medical Resources
Product code: Code LYK
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1993-02-12
Decision date: 1993-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Launa Hills, CA, US

Download summary PDF View on FDA.gov ↗

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