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INTEGRITI PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K980688
510(k) Type
Traditional
Applicant
ALLIANCE INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1999
Days to Decision
386 days
Submission Type
Statement

INTEGRITI PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K980688
510(k) Type
Traditional
Applicant
ALLIANCE INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1999
Days to Decision
386 days
Submission Type
Statement