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PM-1000F+PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K082887
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2009
Days to Decision
108 days
Submission Type
Summary

PM-1000F+PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K082887
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2009
Days to Decision
108 days
Submission Type
Summary