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FDA 510(k), K970889, ULTRASOUND TRANSDUCER DRAPE
FDA 510(k), K970889, ULTRASOUND TRANSDUCER DRAPE
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510(K) Number: K970889
Device Name: ULTRASOUND TRANSDUCER DRAPE
Manufacturer: PROTEK MEDICAL PRODUCTS, INC.
Device Classification Name: drape, surgical
Regulation Number: 878.4370
Classification Product Code: KKX
Date Received: 03/11/1997
Decision Date: 10/20/1997
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ULTRASOUND TRANSDUCER DRAPE
Manufacturer: PROTEK MEDICAL PRODUCTS, INC.
Device Classification Name: drape, surgical
Regulation Number: 878.4370
Classification Product Code: KKX
Date Received: 03/11/1997
Decision Date: 10/20/1997
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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