FDA 510(k), K801757, MMI/GAELTEC CATHETER TIP PRESS. TRANSDU
FDA 510(k), K801757, MMI/GAELTEC CATHETER TIP PRESS. TRANSDU
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510(K) Number: K801757
Device Name: MMI/GAELTEC CATHETER TIP PRESS. TRANSDU
Manufacturer: MEDICAL MEASUREMENTS, INC.
Device Classification Name: recorder, external, pressure, amplifier & transducer
Regulation Number: 876.1725
Classification Product Code: FES
Date Received: 07/28/1980
Decision Date: 08/27/1980
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: MMI/GAELTEC CATHETER TIP PRESS. TRANSDU
Manufacturer: MEDICAL MEASUREMENTS, INC.
Device Classification Name: recorder, external, pressure, amplifier & transducer
Regulation Number: 876.1725
Classification Product Code: FES
Date Received: 07/28/1980
Decision Date: 08/27/1980
Regulation Medical Specialty: Gastroenterology/Urology
- 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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