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

ASO-CHECK

K Number: K831464 · Decision Jun 16, 1983
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
36
Applicant Total
28
Review Days
41

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Basic Information

Device Name
ASO-CHECK
K Number
K831464
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3720
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Diagnostic Technology, Inc.
Date Received
May 6, 1983
Decision Date
June 16, 1983
Product Code
GTQ
Advisory Committee
Microbiology
Review Advisory Committee
IM
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

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K891542 EBNA-CHECK(TM) TEST KIT
K890819 HSV-CHECK(TM) TEST KIT
K871373 EBV-CHECK(TM) TEST KIT (IGG)
K864128 CHLAMYDIA-CHECK(TM) DIRECT & CULTURE CONFIR. KIT
K863408 EBV/VCA-CHECK(TM) ANTIGEN SLIDES
K860586 PHA-2 CONVERSION PROGRAM FOR PLATELET ANALYSIS
K860166 PICOSCALE BLOOD CELL COUNTER, MODEL PS-5
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