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

VZV TEST

K Number: K875358 · Decision Mar 31, 1988
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
10
Applicant Total
57
Review Days
91

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Basic Information

Device Name
VZV TEST
K Number
K875358
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Gull Laboratories, Inc.
Date Received
December 31, 1987
Decision Date
March 31, 1988
Product Code
GQX
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
GQX Antiserum, Cf, Varicella-Zoster

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Other Clearances by Gull Laboratories, Inc.

K Number Device Name
K983541 HSV 1+2 IGG ELISA TEST
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K935730 EBNA IGG ELISA TEST
K940093 EBV-EA(D) IGG ELISA TEST
K941046 VZV IGG ELISA TEST
K941198 EBV LGG ELISA TEST
K932333 PROTECTORAL ULTRASONIC HANDPIECE PROCESSOR
K941624 RUBELLA IGG ELISA TEST
K922758 HSV-1 IGM ELISA TEST -- MODIFICATION
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