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PATIENT MONITOR MODELS PM-2000A, PM-2000A+, PM-2000A PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123048
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2013
Days to Decision
105 days
Submission Type
Summary

PATIENT MONITOR MODELS PM-2000A, PM-2000A+, PM-2000A PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123048
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2013
Days to Decision
105 days
Submission Type
Summary