FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CYCLOSPORIN A (WHOLE BLOOD) CONTROL - LEVELS 1,2,3

K Number: K864456 · Decision May 6, 1987
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
82
Applicant Total
12
Review Days
174

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Basic Information

Device Name
CYCLOSPORIN A (WHOLE BLOOD) CONTROL - LEVELS 1,2,3
K Number
K864456
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Cala Diagnostics
Date Received
November 13, 1986
Decision Date
May 6, 1987
Product Code
LAS
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
LAS Drug Specific Control Materials

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Other Clearances by Cala Diagnostics

K Number Device Name
K944247 CARDIOCHEX CKMB IMMUNOINHIBITION CONTROL
K944246 CARDIOCHEX CKMB MASS MEASUREMENT CONTROL
K944243 CARDIOCHEX
K930874 LD-1 CONTROL-LEVEL 1 & 2
K930875 CKMB CONTROL - LEVEL 1,2,3
K930873 CKMB ISOENZYME CONTROL-LEVEL 1,2.3
K926015 CKMB CONTROL FOR MASS MEASUREMENT-LEVELS 1,2,3
K915503 FIBRINOGEN FDP CONTROL
K912827 SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3
K912826 WHOLE BLOOD ALCOHOL CONTROL, LEVEL 1 & 2
Search all 12 clearances from Cala Diagnostics →