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

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