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

HSV-1 IGG ELISA TEST

K Number: K910954 · Decision May 28, 1991
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
37
Applicant Total
57
Review Days
83

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Basic Information

Device Name
HSV-1 IGG ELISA TEST
K Number
K910954
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3305
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Gull Laboratories, Inc.
Date Received
March 6, 1991
Decision Date
May 28, 1991
Product Code
LGC
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
LGC Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific

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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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K962343 TOXO IGG ELISA TEST
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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