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LaVid FMTS DIAGNOSTIC X-RAY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K180663
510(k) Type
Traditional
Applicant
LIVERMORETECH Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2018
Days to Decision
65 days
Submission Type
Statement

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K180663
510(k) Type
Traditional
Applicant
LIVERMORETECH Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2018
Days to Decision
65 days
Submission Type
Statement