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FDA 510(k), K032821, HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF
FDA 510(k), K032821, HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF
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510(K) Number: K032821
Device Name: HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF
Manufacturer: HYGIA HEALTH SERVICES, INC.
Device Classification Name: reprocessed blood pressure cuff
Regulation Number: 870.1120
Classification Product Code: NPP
Date Received: 09/05/2003
Decision Date: 12/05/2003
Regulation Medical Specialty: Cardiovascular
Device Name: HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF
Manufacturer: HYGIA HEALTH SERVICES, INC.
Device Classification Name: reprocessed blood pressure cuff
Regulation Number: 870.1120
Classification Product Code: NPP
Date Received: 09/05/2003
Decision Date: 12/05/2003
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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