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FDA 510(k) Application Details - K013379
Device Classification Name
Antigens, All Groups, Streptococcus Spp.
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510(K) Number
K013379
Device Name
Antigens, All Groups, Streptococcus Spp.
Applicant
SA SCIENTIFIC, INC.
4919 GOLDEN QUAIL
SAN ANTONIO, TX 78240 US
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Contact
RICARDO R MARTINEZ
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Regulation Number
866.3740
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Classification Product Code
GTY
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More FDA Info for this Product Code
Date Received
10/12/2001
Decision Date
12/12/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
MI - Microbiology
Review Advisory Committee
MI - Microbiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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