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LCV+ VERSION 2

Page Type
Cleared 510(K)
510(k) Number
K993037
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2000
Days to Decision
158 days
Submission Type
Summary

LCV+ VERSION 2

Page Type
Cleared 510(K)
510(k) Number
K993037
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2000
Days to Decision
158 days
Submission Type
Summary