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Lode Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K202979
MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR
December 21, 2020
K852450
LODE COAGULOMETER MODEL LC-6
September 30, 1985
K851097
LODE MODEL CORIVAL ERGOMETER
June 18, 1985