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FDA 510(k), K895920, VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS
FDA 510(k), K895920, VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS
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510(K) Number: K895920
Device Name: VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS
Manufacturer: SOPHIA PESOTCHINSKY
Device Classification Name: Tape And Bandage, Adhesive
Regulation Number: KGX
Classification Product Code: KXA
Date Received: 10/11/1989
Decision Date: 06/06/1991
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS
Manufacturer: SOPHIA PESOTCHINSKY
Device Classification Name: Tape And Bandage, Adhesive
Regulation Number: KGX
Classification Product Code: KXA
Date Received: 10/11/1989
Decision Date: 06/06/1991
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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