ACCUSCOPE(TM) & ACCUSCOPE II(TM)— 510(k) K913365

Substantially Equivalent

Vineland Medical Products, Inc.

FDA 510(k) clearance K913365 for ACCUSCOPE(TM) & ACCUSCOPE II(TM), Substantially Equivalent on 1992-04-27. Applicant: Vineland Medical Products, Inc..

Clearance details

Applicant: Vineland Medical Products, Inc.
Product code: Code HEX
Advisory panel: Obstetrics/Gynecology
Date received: 1991-07-29
Decision date: 1992-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vineland, NJ, US

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