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FDA 510(k), K914241, PIONEER PRO-PUMP DUAL CONTROL
FDA 510(k), K914241, PIONEER PRO-PUMP DUAL CONTROL
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510(K) Number: K914241
Device Name: PIONEER PRO-PUMP DUAL CONTROL
Manufacturer: PIONEER MEDICAL, INC.
Device Classification Name: Curette, Suction, Endometrial (And Accessories)
Regulation Number: 884.1175
Classification Product Code: HHK
Date Received: 09/23/1991
Decision Date: 03/04/1992
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: PIONEER PRO-PUMP DUAL CONTROL
Manufacturer: PIONEER MEDICAL, INC.
Device Classification Name: Curette, Suction, Endometrial (And Accessories)
Regulation Number: 884.1175
Classification Product Code: HHK
Date Received: 09/23/1991
Decision Date: 03/04/1992
Regulation Medical Specialty: Obstetrics/Gynecology
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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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