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FDA 510(k) Application Details - K991667
Device Classification Name
Drape, Surgical
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510(K) Number
K991667
Device Name
Drape, Surgical
Applicant
BROADLINE MEDICAL INDUSTRIES
1432 SHIRE CIRCLE
INVERNESS, IL 60067 US
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Contact
ANNA M RAMZA
Other 510(k) Applications for this Contact
Regulation Number
878.4370
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Classification Product Code
KKX
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More FDA Info for this Product Code
Date Received
05/14/1999
Decision Date
09/27/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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