MODIFIED CURLCATH— 510(k) K872787

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K872787 for MODIFIED CURLCATH, Substantially Equivalent on 1987-08-04. Applicant: Quinton, Inc.. Device class: 1.

Clearance details

Applicant: Quinton, Inc.
Product code: Code GBQ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1987-07-13
Decision date: 1987-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, 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.