PLETHYSMOGRAPH (MDI SYSTEM II)— 510(k) K760504
Substantially EquivalentMarketing Development Intl.
FDA 510(k) clearance K760504 for PLETHYSMOGRAPH (MDI SYSTEM II), Substantially Equivalent on 1976-08-26. Applicant: Marketing Development Intl..
Clearance details
- Applicant
- Marketing Development Intl.
- Product code
- Code JOM
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.