FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HSV-CHECK(TM) TEST KIT

K Number: K890819 · Decision Jun 20, 1989
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
400
Applicant Total
28
Review Days
123

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Basic Information

Device Name
HSV-CHECK(TM) TEST KIT
K Number
K890819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Diagnostic Technology, Inc.
Date Received
February 17, 1989
Decision Date
June 20, 1989
Product Code
HIS
Advisory Committee
Obstetrics/Gynecology
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
HIS Condom

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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
K853036 PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1
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