CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY— 510(k) K950092

Name: FDA 510(k) clearance K950092
Creator: U.S. Food and Drug Administration
Published: 1995-02-27

Unknown

Cypress Medical Products, Ltd.

FDA 510(k) clearance K950092 for CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY, Unknown on 1995-02-27. Applicant: Cypress Medical Products, Ltd.. Device class: 2.

Clearance details

Applicant: Cypress Medical Products, Ltd.
Product code: Code FCM
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1995-01-10
Decision date: 1995-02-27
Decision: Unknown
Clearance type: Traditional
Location: Mc Henry, IL, US

Download summary PDF View on FDA.gov ↗

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