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

CLEARVIEW ADVANCED STREP A , MODEL 737-430

K Number: K091489 · Decision Sep 4, 2009
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
43
Applicant Total
30
Review Days
107

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
CLEARVIEW ADVANCED STREP A , MODEL 737-430
K Number
K091489
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Binax, Inc.
Date Received
May 20, 2009
Decision Date
September 4, 2009
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 Binax, Inc.

K Number Device Name
K090301 BINAXNOW PBP2A TEST, MODEL 890-000
K091766 CLEARVIEW EXACT PBP2A TEST, MODEL 891-000
K090964 BINAXNOX STAPHYLOCOCCUS AUREUS TEST
K083744 BINAXNOW MALARIA POSITIVE CONTROL KIT, MODEL 665-010
K092223 MODIFICATION TO: BINAXNOW INFLUENZA A & B TEST
K080003 BINAXNOW G6PD TEST
K062109 BINAXNOW INFLUENZA A & B TEST
K053126 BINAXNOW INFLUENZA A & B TEST
K041049 BINAXNOW INFLUENZA A & B TEST
K032166 BINAX NOW RSV TEST, MODEL 430-000 AND BINAX NOW NASOPHARYNGEAL SWAB ACCESSORY PACK, MODEL 400-065
Search all 30 clearances from Binax, Inc. →