CARDIOBEEPER CB12/12, MODEL CB12/12— 510(k) K002310
Substantially EquivalentMeridian Medical Technologies , Ltd.
FDA 510(k) clearance K002310 for CARDIOBEEPER CB12/12, MODEL CB12/12, Substantially Equivalent on 2000-10-25. Applicant: Meridian Medical Technologies , Ltd..
Clearance details
- Applicant
- Meridian Medical Technologies , Ltd.
- Product code
- Code DXH
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Belfast, IE
Data sourced from openFDA. This site is unofficial and independent of the FDA.