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

CD3 TRI-COLOR/CD4 R-PE/CD8 FITC MONOCLONAL ANTIBODY COMBINATION

K Number: K951073 · Decision Dec 21, 1995
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
12
Review Days
288

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Basic Information

Device Name
CD3 TRI-COLOR/CD4 R-PE/CD8 FITC MONOCLONAL ANTIBODY COMBINATION
K Number
K951073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Caltag Laboratories, Inc.
Date Received
March 8, 1995
Decision Date
December 21, 1995
Product Code
GKZ
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GKZ Counter, Differential Cell

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GKZ), ordered by most recent decision date.

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Other Clearances by Caltag Laboratories, Inc.

K Number Device Name
K990641 CALTAG FETAL HEMOGLOBIN TEST
K965232 CALTAG CAL-LYSE
K964856 CD3 FITC/CD19 R-PE/CD45 TRI-COLOR MONOCLONAL ANTIBODY COMBINATION
K963954 CD 19 R-PE, CD19 TRI-COLOR MONOCLONAL ANTIBODY
K950918 CD3 FITC/CD4 R-PE MONOCLONAL ANTIBODY COMBINATION
K950917 CD3 FITC/CD8 R-PE/CD45 TRI-COLOR MONOCLONAL ANTIBODY COMBINATION
K950916 CD3 FITC/CD8 R-PE MONOCLONAL ANTIBODY COMBINATION
K950919 CD3 FITC/CD4 R-PE/CD45 TRI-COLOR MONOCLONAL ANTIBODY COMBINATION
K944127 CALTAG CD3 FITC, R-PE, TRI-COLOR MONOCLONAL ANTIBODY
K944128 CALTAG CD4 R-PE MONOCLONAL ANTIBODY
Search all 12 clearances from Caltag Laboratories, Inc. →