FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SAS STREPALERT

K Number: K013379 · Decision Dec 12, 2001
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
43
Applicant Total
199
Review Days
61

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SAS STREPALERT
K Number
K013379
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sa Scientific, Inc.
Date Received
October 12, 2001
Decision Date
December 12, 2001
Product Code
GTY
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GTY Antigens, All Groups, Streptococcus Spp.

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GTY), ordered by most recent decision date.

View all

Other Clearances by Sa Scientific, Inc.

K Number Device Name
K100227 SAS FLUALERT A&B, SAS INFLUENZA A TEST
K080380 SAS INFLUENZA A & B TEST
K041439 SAS INFLUENZA B TEST
K041441 SAS INFLUENZA A TEST
K030628 SAS RSV CONTROL KIT
K022845 SAS RSV TEST
K022683 SAS BLOOD/SERUM/URINE/URINE HCG
K023270 SAS STREPALERT
K020438 SAS VALUE HCG
K010522 SUREVUE URINE HCG
Search all 199 clearances from Sa Scientific, Inc. →