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FDA 510(k), K933772, PUNCH SURGICAL
FDA 510(k), K933772, PUNCH SURGICAL
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510(K) Number: K933772
Device Name: PUNCH SURGICAL
Manufacturer: MAHE-MEDIZINTECHNIK
Device Classification Name: orthopedic manual surgical instrument
Regulation Number: 888.4540
Classification Product Code: LXH
Date Received: 07/29/1993
Decision Date: 02/01/1994
Regulation Medical Specialty: Orthopedic
Device Name: PUNCH SURGICAL
Manufacturer: MAHE-MEDIZINTECHNIK
Device Classification Name: orthopedic manual surgical instrument
Regulation Number: 888.4540
Classification Product Code: LXH
Date Received: 07/29/1993
Decision Date: 02/01/1994
Regulation Medical Specialty: Orthopedic
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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