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FDA 510(k), K123803, REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
FDA 510(k), K123803, REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
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510(K) Number: K123803
Device Name: REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
Manufacturer: REVERSE MEDICAL CORPORATION
Device Classification Name: device, vascular, for promoting embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 12/10/2012
Decision Date: 07/02/2013
Regulation Medical Specialty: Cardiovascular
Device Name: REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
Manufacturer: REVERSE MEDICAL CORPORATION
Device Classification Name: device, vascular, for promoting embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 12/10/2012
Decision Date: 07/02/2013
Regulation Medical Specialty: Cardiovascular
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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