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

CYCLOSPORINE (WHOLE BLOOD) CONTROL-PEDIATRIC LEVEL

K Number: K932662 · Decision Jul 26, 1993
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
82
Applicant Total
16
Review Days
54

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Basic Information

Device Name
CYCLOSPORINE (WHOLE BLOOD) CONTROL-PEDIATRIC LEVEL
K Number
K932662
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
More Diagnostics
Date Received
June 2, 1993
Decision Date
July 26, 1993
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 510(k) clearances with the same product code (LAS), ordered by most recent decision date.

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Other Clearances by More Diagnostics

K Number Device Name
K072257 MYCOPHENOLIC ACID CONTROL, LEVEL 1, 2, 3, 4, 4-LEVEL
K050125 RAP/TAC/CSA CONTROL - LEVEL 1,2,3,4
K982845 CARDIAC MARKERS CONTROL (SINGLE USE)-LEVELS, 1,2,3, MODELS NUMBER 175-1, 175-2, 175-3
K980331 IMMUNOSUPPRESSANT (WHOLE BLOOD) CONTROL, LEVEL 1 250-1, IMMUNOSUPPRESSANT (WHOLE BLOOS) CONTROL, LEVEL 2, 250-2, IMMUN\S
K972976 CARDIAC MARKERS CONTROL - LEVEL 1, LEVEL 2, LEVEL 3, TRI-LEVEL
K970778 LEAD CONTROL (WHOLE BLOOD) LEVELS 1,2,3,4
K946193 FIBRINOGEN CONTROL (HUMAN) LEVEL 1, 2, 3
K943571 MULTI-LEVEL CONTROL FOR FIBRIN DEGRADATION PRODUCTS
K944999 SERUM BILIRUBIN CONTROL- LEVEL 1, 2 AND 3
K941876 WHOLE BLOOD VOLATILES CONTROL, LEVELS 1 AND 2
Search all 16 clearances from More Diagnostics →