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FDA 510(k) Application Details - K955150
Device Classification Name
Tube, Aspirating, Flexible, Connecting
More FDA Info for this Device
510(K) Number
K955150
Device Name
Tube, Aspirating, Flexible, Connecting
Applicant
BIO-MEDICAL DEVICES, INC.
1752-A LANGLEY AVE.
IRVINE, CA 92614 US
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Contact
NICK HERBERT
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Regulation Number
880.6740
More FDA Info for this Regulation Number
Classification Product Code
BYY
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More FDA Info for this Product Code
Date Received
11/13/1995
Decision Date
01/23/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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