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FDA 510(k) Application Details - K021076
Device Classification Name
Mask, Surgical
More FDA Info for this Device
510(K) Number
K021076
Device Name
Mask, Surgical
Applicant
PRIMELINE MEDICAL PRODUCTS, INC.
10707-100TH AVE., SUITE 300
EDMONTON, ALBERTA T5J 3M1 CA
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Contact
BRENDA LEE
Other 510(k) Applications for this Contact
Regulation Number
878.4040
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Classification Product Code
FXX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/03/2002
Decision Date
04/16/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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