CATHETER PLUG/PROTECTOR— 510(k) K896806

Name: FDA 510(k) clearance K896806
Creator: U.S. Food and Drug Administration
Published: 1990-02-26

Substantially Equivalent

Westmark, Sterile Packing Systems, Inc. (Sps)

FDA 510(k) clearance K896806 for CATHETER PLUG/PROTECTOR, Substantially Equivalent on 1990-02-26. Applicant: Westmark, Sterile Packing Systems, Inc. (Sps). Device class: 2.

Clearance details

Applicant: Westmark, Sterile Packing Systems, Inc. (Sps)
Product code: Code KNY
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1989-12-01
Decision date: 1990-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, 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.