Last synced on 25 January 2026 at 3:41 am

MODIFICATION TO 3.0T SIGNA VH/I MAGNETIC RESONANCE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003575
510(k) Type
Traditional
Applicant
GE Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2001
Days to Decision
58 days
Submission Type
Summary

MODIFICATION TO 3.0T SIGNA VH/I MAGNETIC RESONANCE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003575
510(k) Type
Traditional
Applicant
GE Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2001
Days to Decision
58 days
Submission Type
Summary