LAKE FOLEY CATHETERIZATION TRAY— 510(k) K883610

Name: FDA 510(k) clearance K883610
Creator: U.S. Food and Drug Administration
Published: 1988-10-12

Substantially Equivalent

Lake Medical Products, Inc.

FDA 510(k) clearance K883610 for LAKE FOLEY CATHETERIZATION TRAY, Substantially Equivalent on 1988-10-12. Applicant: Lake Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Lake Medical Products, Inc.
Product code: Code FCN
Device class: Class 2
Regulation: 21 CFR 876.5250
Advisory panel: Gastroenterology, Urology
Date received: 1988-08-22
Decision date: 1988-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

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