FDA 510(k), K960673, OSAP
FDA 510(k), K960673, OSAP
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510(K) Number: K960673
Device Name: OSAP
Manufacturer:
Device Classification Name: Device, Jaw Repositioning
Regulation Number: 872.5570
Classification Product Code: LQZ
Date Received: 02/20/1996
Decision Date: 05/09/1996
Regulation Medical Specialty: Dental
Device Name: OSAP
Manufacturer:
Device Classification Name: Device, Jaw Repositioning
Regulation Number: 872.5570
Classification Product Code: LQZ
Date Received: 02/20/1996
Decision Date: 05/09/1996
Regulation Medical Specialty: Dental