PENLON I.D.P. PRESSSURE FAILURE ALARM— 510(k) K801254

Substantially Equivalent

Penlon, 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
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