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

DELFIA DIGOXIN

K Number: K861195 · Decision Jul 11, 1986
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
84
Applicant Total
52
Review Days
102

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Basic Information

Device Name
DELFIA DIGOXIN
K Number
K861195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3320
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Lkb Instruments, Inc.
Date Received
March 31, 1986
Decision Date
July 11, 1986
Product Code
KXT
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
KXT Enzyme Immunoassay, Digoxin

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Other Clearances by Lkb Instruments, Inc.

K Number Device Name
K874094 1205 BETAPLATE LIQUID SCINTILLATION COUNTER
K872955 DELFIA(TM) FERRITIN KIT
K871303 DELFIA(TM) THYROXINE (T4) KIT
K871599 DELFIA(TM) HIGE KIT
K871644 DELFIA (TM) HTSH KIT
K864452 DELFIA(TM) TRIIODOTHYRONINE (T3) KIT
K864733 LKB 2260 MACROTOME
K862848 LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110
K863422 DELFIA(TM) CORTISOL KIT
K862044 DELFIA (TM) HCG KIT
Search all 52 clearances from Lkb Instruments, Inc. →