INTRODUCTION/DRAINAGE CATHETER & ACCESS— 510(k) K881873

Name: FDA 510(k) clearance K881873
Creator: U.S. Food and Drug Administration
Published: 1988-05-18

Substantially Equivalent

Sheridan Catheter Corp.

FDA 510(k) clearance K881873 for INTRODUCTION/DRAINAGE CATHETER & ACCESS, Substantially Equivalent on 1988-05-18. Applicant: Sheridan Catheter Corp.. Device class: 1.

Clearance details

Applicant: Sheridan Catheter Corp.
Product code: Code GBS
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1988-05-03
Decision date: 1988-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Argyle, NY, US

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