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

FERRITIN CONTROL - LEVEL 1, 2, 3

K Number: K946266 · Decision Feb 10, 1995
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
17
Review Days
49

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Basic Information

Device Name
FERRITIN CONTROL - LEVEL 1, 2, 3
K Number
K946266
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Clinical Controls, Inc.
Date Received
December 23, 1994
Decision Date
February 10, 1995
Product Code
DGD
Advisory Committee
Immunology
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
DGD Igg, Ferritin, Antigen, Antiserum, Control

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Other Clearances by Clinical Controls, Inc.

K Number Device Name
K964278 WHOLE BLOOD GLUCOSE CONTROL LEVEL 1,2,AND 3/WHOLE BLOOD GLUCOSE LINEARITY CONTROL-LEVEL1,2,3,4,5,AND 6
K962432 LIQUISPEX URINE (MICRO)ALBUMIN CONTROL
K955690 AQUEOUS ETHANOL/AMMONIA CONTROL LEVEL 1, 2, & 3
K955691 SERUM VOLATILES CONTROL LEVEL 1 & 2
K946265 FIBRINOGEN HIGH ABNORMAL CONTROL - LEVEL 3
K935598 PLASMA FIBRINOGEN CONTROL LEVEL 1/LEVEL 2
K946049 LIQUISPEX(TM) LIQUID B2M/CRP CONTROL LEVEL 1 AND 2
K946048 LIQUISPEX(TM) LIQUID B2M CONTROL LEVEL 1 AND 2
K946050 LIQUISPEX(TM) LIQUID CRP CONTROL LEVEL 1 AND 2
K946144 LIQUISPEX(TM) URINE ETHANOL CONTROL
Search all 17 clearances from Clinical Controls, Inc. →