OMNITECH RESECTOSCOPE ROLLER ELECTRODE— 510(k) K981463

Substantially Equivalent

Omnitech Systems, Inc.

FDA 510(k) clearance K981463 for OMNITECH RESECTOSCOPE ROLLER ELECTRODE, Substantially Equivalent on 1998-07-17. Applicant: Omnitech Systems, Inc..

Clearance details

Applicant: Omnitech Systems, Inc.
Product code: Code KNF
Advisory panel: Obstetrics/Gynecology
Date received: 1998-04-23
Decision date: 1998-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valparaiso, IN, US

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