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

STAINING SYSTEM FOR PNEUMOCYSTIS CARINII

K Number: K905504 · Decision Jun 28, 1991
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
6
Applicant Total
54
Review Days
203

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Basic Information

Device Name
STAINING SYSTEM FOR PNEUMOCYSTIS CARINII
K Number
K905504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Dako Corp.
Date Received
December 7, 1990
Decision Date
June 28, 1991
Product Code
LYF
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
LYF Pneumocystis Carinii

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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. →