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FDA 510(k) Application Details - K023266
Device Classification Name
Gown, Surgical
More FDA Info for this Device
510(K) Number
K023266
Device Name
Gown, Surgical
Applicant
PRIMELINE MEDICAL PRODUCTS, INC.
1591 FOUR ROD RD.
ALDEN, NY 14004 US
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DAVID POWER
Other 510(k) Applications for this Contact
Regulation Number
878.4040
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Classification Product Code
FYA
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More FDA Info for this Product Code
Date Received
09/30/2002
Decision Date
11/08/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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