VANCE URETHAL DILATOR SET— 510(k) K810371

Substantially Equivalent

Vance Products, Inc.

FDA 510(k) clearance K810371 for VANCE URETHAL DILATOR SET, Substantially Equivalent on 1981-03-20. Applicant: Vance Products, Inc..

Clearance details

Applicant: Vance Products, Inc.
Product code: Code KOE
Advisory panel: Gastroenterology, Urology
Date received: 1981-02-12
Decision date: 1981-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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