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DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992638
510(k) Type
Traditional
Applicant
Critikon Company, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2000
Days to Decision
202 days
Submission Type
Summary

DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992638
510(k) Type
Traditional
Applicant
Critikon Company, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2000
Days to Decision
202 days
Submission Type
Summary