DeviceClearance

PENLON IDP PRESSURE FAILURE ALARM— 510(k) K894689

Substantially Equivalent

Penlon, Inc.

FDA 510(k) clearance K894689 for PENLON IDP PRESSURE FAILURE ALARM, Substantially Equivalent on 1989-08-10. 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
Riverside, CA, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.