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Lkb Instruments, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
52
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K8740941205 BETAPLATE LIQUID SCINTILLATION COUNTERNovember 4, 1987
K872955DELFIA(TM) FERRITIN KITAugust 21, 1987
K871303DELFIA(TM) THYROXINE (T4) KITJune 17, 1987
K871599DELFIA(TM) HIGE KITJune 12, 1987
K871644DELFIA (TM) HTSH KITMay 12, 1987
K864452DELFIA(TM) TRIIODOTHYRONINE (T3) KITFebruary 2, 1987
K864733LKB 2260 MACROTOMEJanuary 5, 1987
K862848LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110December 18, 1986
K863422DELFIA(TM) CORTISOL KITSeptember 26, 1986
K861195DELFIA DIGOXINJuly 11, 1986
K862044DELFIA (TM) HCG KITJuly 11, 1986
K862043DELFIA (TM) HFSH KITJune 24, 1986
K861542DELFIA (TM) HUMAN PROLACTINJune 17, 1986
K861194ULTROSPEC K KINETICS SPECTROPHOTOMETERApril 24, 1986
K855173DELFIA TM HLH KITFebruary 28, 1986
K852760LBK 1244 DELFIA HCG KITDecember 5, 1985
K852538LKB 4057 ULTROSPEC II ESeptember 30, 1985
K8524341208 BETACORD AND 1208 BETCORD MAugust 2, 1985
K851120DELFIA HTSH KITMay 31, 1985
K851984LKB-WALLAC 1230 ARCUS FLUOROMETERMay 24, 1985