PENLON I.D.P. PRESSSURE FAILURE ALARM— 510(k) K801254
Substantially EquivalentPenlon, Inc.
FDA 510(k) clearance K801254 for PENLON I.D.P. PRESSSURE FAILURE ALARM, Substantially Equivalent on 1980-06-09. Applicant: Penlon, Inc..
Clearance details
- Applicant
- Penlon, 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.