VERRES NEEDLE— 510(k) K942484

Substantially Equivalent

Linvatec Corp.

FDA 510(k) clearance K942484 for VERRES NEEDLE, Substantially Equivalent on 1994-06-24. Applicant: Linvatec Corp..

Clearance details

Applicant: Linvatec Corp.
Product code: Code FHO
Advisory panel: Gastroenterology, Urology
Date received: 1994-05-25
Decision date: 1994-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

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