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

ASO SURE

K Number: K820785 · Decision Apr 8, 1982
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
36
Applicant Total
57
Review Days
16

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Basic Information

Device Name
ASO SURE
K Number
K820785
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3720
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Analytical Products, Inc.
Date Received
March 23, 1982
Decision Date
April 8, 1982
Product Code
GTQ
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
GTQ Antistreptolysin - Titer/Streptolysin O Reagent

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GTQ), 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. →