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

QUALITROL CARDIAC MARKER CONTROL, LEVELS, 1,2 AND 3

K Number: K993715 · Decision Nov 16, 1999
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
5
Review Days
13

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Basic Information

Device Name
QUALITROL CARDIAC MARKER CONTROL, LEVELS, 1,2 AND 3
K Number
K993715
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Seracare Technology
Date Received
November 3, 1999
Decision Date
November 16, 1999
Product Code
JJT
Advisory Committee
Clinical Chemistry
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
JJT Enzyme Controls (Assayed And Unassayed)

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Other Clearances by Seracare Technology

K Number Device Name
K992939 QUALITROL IMMUNOASSAY PLUS CONTROL, LEVELS 1,2 AND 3
K993631 QUALITROL TUMOR MARKER CONTROL, LEVELS 1 AND 2
K992770 QUALITROL IMMUNOLOGY CONTROL, LEVEL 1, 2 AND 3
K992395 URINE DRUG SCREENING CONTROL