FORDER RETRACTOR— 510(k) K811973

Substantially Equivalent

Surgemed Marketing, Inc.

FDA 510(k) clearance K811973 for FORDER RETRACTOR, Substantially Equivalent on 1981-07-31. Applicant: Surgemed Marketing, Inc.. Device class: 1.

Clearance details

Applicant: Surgemed Marketing, Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1981-07-10
Decision date: 1981-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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