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FDA 510(k), K883968, TENDERFOOT
FDA 510(k), K883968, TENDERFOOT
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510(K) Number: K883968
Device Name: TENDERFOOT
Manufacturer: INTERNATIONAL TECHNIDYNE CORP.
Device Classification Name: single use only blood lancet with an integral sharps injury prevention feature
Regulation Number: 878.4850
Classification Product Code: FMK
Date Received: 09/20/1988
Decision Date: 12/01/1988
Regulation Medical Specialty: General & Plastic Surgery
Device Name: TENDERFOOT
Manufacturer: INTERNATIONAL TECHNIDYNE CORP.
Device Classification Name: single use only blood lancet with an integral sharps injury prevention feature
Regulation Number: 878.4850
Classification Product Code: FMK
Date Received: 09/20/1988
Decision Date: 12/01/1988
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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