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

Name: FDA 510(k) clearance K913365
Creator: U.S. Food and Drug Administration
Published: 1992-04-27

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.. Device class: 2.

Clearance details

Applicant: Vineland Medical Products, Inc.
Product code: Code HEX
Device class: Class 2
Regulation: 21 CFR 884.1630
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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