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

API-CTS STREPTOCOCCUS

K Number: K801951 · Decision Sep 26, 1980
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
243
Applicant Total
57
Review Days
39

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Basic Information

Device Name
API-CTS STREPTOCOCCUS
K Number
K801951
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Analytical Products, Inc.
Date Received
August 18, 1980
Decision Date
September 26, 1980
Product Code
JTO
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
JTO Discs, Strips And Reagents, Microorganism Differentiation

Similar 510(k) Clearances

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

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Other Clearances by Analytical Products, Inc.

K Number Device Name
K924814 API 20E/UNISCEPT 20E
K923684 API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC
K922926 API UNISCEPT KB/TYPE 2 AND 3
K901559 MODIFICATION TO API UNISCEPT 20GP
K901390 DMAC INDOLE REAGENT
K895796 API UNISCEPT KB
K884510 MODIFICATION MICRO-MIC
K884509 MODIFICATION MIC/API UNISCEPT(R)
K880598 MODIFICATIONS TO API UNISCEPT (R) KB
K874466 API UNISCEPT(R) MICRO-MIC(R) SYSTEM/UNISCEPT MIC
Search all 57 clearances from Analytical Products, Inc. →