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AIRWAY PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K810753
510(k) Type
Traditional
Applicant
IMPACT INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1981
Days to Decision
11 days

AIRWAY PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K810753
510(k) Type
Traditional
Applicant
IMPACT INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1981
Days to Decision
11 days