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

ANA TEST (MOUSE LIVER SUBSTRATE)

K Number: K820265 · Decision Feb 12, 1982
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
15
Review Days
10

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Basic Information

Device Name
ANA TEST (MOUSE LIVER SUBSTRATE)
K Number
K820265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Meloy Laboratories, Inc.
Date Received
February 2, 1982
Decision Date
February 12, 1982
Product Code
DHN
Advisory Committee
Immunology
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
DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

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Other Clearances by Meloy Laboratories, Inc.

K Number Device Name
K852033 SS-A(RO) & SS-B(LA) ANTIBODY ASSAY
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K841708 MELOY IMMUNOSTAT MONOCLONAL FACTOR VIII
K842247 MELOY AUTOANTIBODY TEST SYS
K831292 ANTI-ENA TEST
K820005 TOTAL HEMOLYTIC COMPLEMENT TEST KIT
K811178 HUMAN IGG-ALBUMIN TEST KIT
K792562 IMMUNOSTAT TSH TEST
K791493 ANTI-NUCLEAR ANTIBODY TEST
K791065 IMMUNOSPOT TSH TEST
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