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REXTAR, REXTAR LCD

Page Type
Cleared 510(K)
510(k) Number
K122016
510(k) Type
Traditional
Applicant
META BIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2013
Days to Decision
234 days
Submission Type
Summary

REXTAR, REXTAR LCD

Page Type
Cleared 510(K)
510(k) Number
K122016
510(k) Type
Traditional
Applicant
META BIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2013
Days to Decision
234 days
Submission Type
Summary