VENTI-MONITOR MODEL 101— 510(k) K812041
Substantially EquivalentMedix Medical Electronics (U.S.A.), Inc.
FDA 510(k) clearance K812041 for VENTI-MONITOR MODEL 101, Substantially Equivalent on 1981-09-25. Applicant: Medix Medical Electronics (U.S.A.), Inc..
Clearance details
- Applicant
- Medix Medical Electronics (U.S.A.), Inc.
- Product code
- Code CAP
- Advisory panel
- Anesthesiology
- 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.