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FDA 510(k), K112341, SNAP WOUND CARE SYSTEM
FDA 510(k), K112341, SNAP WOUND CARE SYSTEM
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510(K) Number: K112341
Device Name: SNAP WOUND CARE SYSTEM
Manufacturer: SPIRACUR, INC.
Device Classification Name: negative pressure wound therapy non-powered suction apparatus
Regulation Number: 878.4683
Classification Product Code: OKO
Date Received: 08/15/2011
Decision Date: 08/29/2011
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SNAP WOUND CARE SYSTEM
Manufacturer: SPIRACUR, INC.
Device Classification Name: negative pressure wound therapy non-powered suction apparatus
Regulation Number: 878.4683
Classification Product Code: OKO
Date Received: 08/15/2011
Decision Date: 08/29/2011
Regulation Medical Specialty: General & Plastic Surgery
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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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