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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Circuit, Breathing (W Connector, Adaptor, Y Piece)
510(k) Number K870859
Device Name BAG-TAIL BLEED VALVE
Applicant
Dryden Corp.
10640 E. 59th St.
P.O. Box 36038
Indianapolis,  IN  46236
Applicant Contact PAUL E DRYDEN
Correspondent
Dryden Corp.
10640 E. 59th St.
P.O. Box 36038
Indianapolis,  IN  46236
Correspondent Contact PAUL E DRYDEN
Regulation Number868.5240
Classification Product Code
CAI  
Date Received03/03/1987
Decision Date 08/03/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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