FOLEY CATHETERIZATION TRAY— 510(k) K790254

Name: FDA 510(k) clearance K790254
Creator: U.S. Food and Drug Administration
Published: 1979-04-10

Substantially Equivalent

Snyder Laboratories, Inc.

FDA 510(k) clearance K790254 for FOLEY CATHETERIZATION TRAY, Substantially Equivalent on 1979-04-10. Applicant: Snyder Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Snyder Laboratories, Inc.
Product code: Code FCM
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1979-02-06
Decision date: 1979-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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