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

DAKO ITA, IMMUNOGLOBULIN M (IGM)

K Number: K862184 · Decision Aug 19, 1986
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
6
Applicant Total
54
Review Days
71

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Basic Information

Device Name
DAKO ITA, IMMUNOGLOBULIN M (IGM)
K Number
K862184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Dako Corp.
Date Received
June 9, 1986
Decision Date
August 19, 1986
Product Code
DAH
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
DAH Gamma Globulin, Antigen, Antiserum, Control

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Other Clearances by Dako Corp.

K Number Device Name
K020023 DAKO MONOCLONAL MOUSE ANTI-HUMAN PROGESTERONE RECEPTOR, CLONE PGR 636, ANTIBODY FOR IMMUNOENZYMATIC STAINING
K993957 DAKO MONOCLONAL MOUSE ANTI-HUMAN ESTROGEN RECEPTOR
K991402 DAKO MOUSE ANTI-HUMAN T-CELL, CD3/RPE-CY5, CLONE UCHT1 & DAKO MOUSE ANTI-HUMAN T-CELL, CD3/RPE, CLONE UCHT1
K991454 MOUSE IGG1 NEGATIVE CONTROLS
K980635 DAKO MOUSE ANTI-HUMAN B-CELL, CD19/RPE-CY5, CLONE HD37
K971905 DAKO MOUSE ANTI HUMAN CYTOKERATIN, HIGH MOLECULAR WEIGHT, CLONE 34BE12, MONOCLONAL ANTIBODY FOR IMMUNOENZYMATIC STAINING
K965022 MONOCLONAL MOUSE ANTI-HUMAN CD30, KI-1 ANTIGEN, BER-H2 ANTIBODY FOR IMMUNOENZYMATIC STAINING (PRODUCT CODE NO. MO751)
K964974 MOUSE ANTI-HUMAN CD45, LEUCOCYTE COMMON ANTIGEN (LCA)/FITC AND CD14, MONOCYTE/RPE
K961701 MOUSE ANTI-HUMAN CD3, T-CELL, FITC AND CD4, T-CELL, (HELPER/INDUCER) RPE
K951965 DAKO LABELED STREPTAVIDIN-BIOTIN 2 KIT, AND ENVISION
Search all 54 clearances from Dako Corp. →