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

MULTI-LEVEL CONTROL FOR FIBRIN DEGRADATION PRODUCTS

K Number: K943571 · Decision Jun 15, 1995
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
56
Applicant Total
16
Review Days
331

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Basic Information

Device Name
MULTI-LEVEL CONTROL FOR FIBRIN DEGRADATION PRODUCTS
K Number
K943571
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7320
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
More Diagnostics
Date Received
July 19, 1994
Decision Date
June 15, 1995
Product Code
DAP
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
DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control

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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
K944999 SERUM BILIRUBIN CONTROL- LEVEL 1, 2 AND 3
K941876 WHOLE BLOOD VOLATILES CONTROL, LEVELS 1 AND 2
K941698 SERUM VOLATILES CONTROL - LEVELS 1 AND 2
Search all 16 clearances from More Diagnostics →