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

ANTI-MITOCHONDRIAL

K Number: K771155 · Decision Aug 4, 1977
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
5
Applicant Total
15
Review Days
37

Basic Information

Device Name
ANTI-MITOCHONDRIAL
K Number
K771155
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5120
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
MELOY LABORATORIES, INC.
Date Received
June 28, 1977
Decision Date
August 4, 1977
Product Code
DBE
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
DBE Antismooth Muscle Antibody, Indirect Immunofluorescent, Antigen, Control

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K842247 MELOY AUTOANTIBODY TEST SYS
K831292 ANTI-ENA TEST
K820265 ANA TEST (MOUSE LIVER SUBSTRATE)
K820005 TOTAL HEMOLYTIC COMPLEMENT TEST KIT
K811178 HUMAN IGG-ALBUMIN TEST KIT
K792562 IMMUNOSTAT TSH TEST
K791493 ANTI-NUCLEAR ANTIBODY TEST
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