LIDCORAPID V2 MONITOR— 510(k) K122247
Substantially EquivalentLidco, Ltd.
FDA 510(k) clearance K122247 for LIDCORAPID V2 MONITOR, Substantially Equivalent on 2013-03-20. Applicant: Lidco, Ltd..
Clearance details
- Applicant
- Lidco, Ltd.
- Product code
- Code DXG
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- London, GB
Data sourced from openFDA. This site is unofficial and independent of the FDA.