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PENLON BREATHING SYSTEM PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K902381
510(k) Type
Traditional
Applicant
PENLON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
79 days

PENLON BREATHING SYSTEM PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K902381
510(k) Type
Traditional
Applicant
PENLON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
79 days