FDA 510(k) K830332, BUDDE-HALO RETRACTOR, by Ohio Medical Instrument Co., Inc.
FDA 510(k) K830332, BUDDE-HALO RETRACTOR, by Ohio Medical Instrument Co., Inc.
Device Name: BUDDE-HALO RETRACTOR
Manufacturer: Ohio Medical Instrument Co., Inc.
Device Classification Name: Retractor, Self-Retaining, For Neurosurgery
Regulation Number: GZT
Classification Product Code: KXA
Date Received: 02/01/1983
Decision Date: 03/02/1983
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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