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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 K932485
Device Name PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS
Applicant
PRECISION MED PRODUCTS, LTD.
30 ROBB HILL RD.
SUITE B
MARRTINSVILLE,  IN  46151
Applicant Contact ROD FYE
Correspondent
PRECISION MED PRODUCTS, LTD.
30 ROBB HILL RD.
SUITE B
MARRTINSVILLE,  IN  46151
Correspondent Contact ROD FYE
Regulation Number868.5240
Classification Product Code
CAI  
Date Received05/24/1993
Decision Date 07/13/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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