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FDA 510(k), K940973, MULLAN GANGLION MICROCOMPRESSION SET
FDA 510(k), K940973, MULLAN GANGLION MICROCOMPRESSION SET
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510(K) Number: K940973
Device Name: MULLAN GANGLION MICROCOMPRESSION SET
Manufacturer: COOK, INC.
Device Classification Name: instrument, surgical, non-powered
Regulation Number: 882.4535
Classification Product Code: HAO
Date Received: 03/03/1994
Decision Date: 09/29/1995
Regulation Medical Specialty: Neurology
Device Name: MULLAN GANGLION MICROCOMPRESSION SET
Manufacturer: COOK, INC.
Device Classification Name: instrument, surgical, non-powered
Regulation Number: 882.4535
Classification Product Code: HAO
Date Received: 03/03/1994
Decision Date: 09/29/1995
Regulation Medical Specialty: Neurology
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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