FDA 510(k), K791914, 3-WAY STOPCOCK W/MALE LOCKING LUER ADA.
FDA 510(k), K791914, 3-WAY STOPCOCK W/MALE LOCKING LUER ADA.
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510(K) Number: K791914
Device Name: 3-WAY STOPCOCK W/MALE LOCKING LUER ADA.
Manufacturer: ABBOTT LABORATORIES
Device Classification Name: adaptor, stopcock, manifold, fitting, cardiopulmonary bypass
Regulation Number: 870.4290
Classification Product Code: DTL
Date Received: 09/25/1979
Decision Date: 10/11/1979
Regulation Medical Specialty: Cardiovascular
Device Name: 3-WAY STOPCOCK W/MALE LOCKING LUER ADA.
Manufacturer: ABBOTT LABORATORIES
Device Classification Name: adaptor, stopcock, manifold, fitting, cardiopulmonary bypass
Regulation Number: 870.4290
Classification Product Code: DTL
Date Received: 09/25/1979
Decision Date: 10/11/1979
Regulation Medical Specialty: Cardiovascular
- 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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