Last synced on 25 January 2026 at 3:41 am

DINAMAP PRO 1000 MONITOR, MODEL 1000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012915
510(k) Type
Traditional
Applicant
Ge Medical Systems Information Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
203 days
Submission Type
Summary

DINAMAP PRO 1000 MONITOR, MODEL 1000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012915
510(k) Type
Traditional
Applicant
Ge Medical Systems Information Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
203 days
Submission Type
Summary