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MODEL 2120IS SERIES MATERNAL/FETAL MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021135
510(k) Type
Special
Applicant
Ge Medical Systems Information Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2002
Days to Decision
30 days
Submission Type
Summary

MODEL 2120IS SERIES MATERNAL/FETAL MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021135
510(k) Type
Special
Applicant
Ge Medical Systems Information Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2002
Days to Decision
30 days
Submission Type
Summary