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FDA 510(k), K955246, ECOGEL 200 ULTRASOUND GEL
FDA 510(k), K955246, ECOGEL 200 ULTRASOUND GEL
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510(K) Number: K955246
Device Name: ECOGEL 200 ULTRASOUND GEL
Manufacturer: ECO-MED PHARMACEUTICALS, INC.
Device Classification Name: transducer, ultrasonic, diagnostic
Regulation Number: 892.1570
Classification Product Code: ITX
Date Received: 11/15/1995
Decision Date: 02/21/1996
Regulation Medical Specialty: Radiology
Device Name: ECOGEL 200 ULTRASOUND GEL
Manufacturer: ECO-MED PHARMACEUTICALS, INC.
Device Classification Name: transducer, ultrasonic, diagnostic
Regulation Number: 892.1570
Classification Product Code: ITX
Date Received: 11/15/1995
Decision Date: 02/21/1996
Regulation Medical Specialty: Radiology
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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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