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FDA 510(k), K032119, PARAGON MEDICAL SURGICAL INSTRUMENT DELIVERY SYSTEM VARIOUS
FDA 510(k), K032119, PARAGON MEDICAL SURGICAL INSTRUMENT DELIVERY SYSTEM VARIOUS
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510(K) Number: K032119
Device Name: PARAGON MEDICAL SURGICAL INSTRUMENT DELIVERY SYSTEM VARIOUS
Manufacturer: PARAGON MEDICAL, INC.
Device Classification Name: sterilization wrap containers, trays, cassettes & other accessories
Regulation Number: 880.6850
Classification Product Code: KCT
Date Received: 07/09/2003
Decision Date: 10/29/2003
Regulation Medical Specialty: General Hospital
Device Name: PARAGON MEDICAL SURGICAL INSTRUMENT DELIVERY SYSTEM VARIOUS
Manufacturer: PARAGON MEDICAL, INC.
Device Classification Name: sterilization wrap containers, trays, cassettes & other accessories
Regulation Number: 880.6850
Classification Product Code: KCT
Date Received: 07/09/2003
Decision Date: 10/29/2003
Regulation Medical Specialty: General Hospital
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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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