Lode B.V.
FDA Regulatory Profile
Lode B.V. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 21, 2020.
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 |