ECG MODULATOR— 510(k) K922412
Substantially EquivalentMaguire Ent., Inc.
FDA 510(k) clearance K922412 for ECG MODULATOR, Substantially Equivalent on 1992-07-06. Applicant: Maguire Ent., Inc..
Clearance details
- Applicant
- Maguire Ent., Inc.
- Product code
- Code DXH
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fort Lauderdale, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.