PCX-100 PATIENT INPUT LEADWIRE— 510(k) K851632
Substantially EquivalentEaton Medical Group
FDA 510(k) clearance K851632 for PCX-100 PATIENT INPUT LEADWIRE, Substantially Equivalent on 1985-11-08. Applicant: Eaton Medical Group.
Clearance details
- Applicant
- Eaton Medical Group
- Product code
- Code DRW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Eaton, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.