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PENLON IDP PRESSURE FAILURE ALARM

Page Type
Cleared 510(K)
510(k) Number
K894689
510(k) Type
Traditional
Applicant
PENLON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1989
Days to Decision
17 days

PENLON IDP PRESSURE FAILURE ALARM

Page Type
Cleared 510(K)
510(k) Number
K894689
510(k) Type
Traditional
Applicant
PENLON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1989
Days to Decision
17 days