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FLEXMAP 3D

Page Type
Cleared 510(K)
510(k) Number
K133302
510(k) Type
Traditional
Applicant
LUMINEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2014
Days to Decision
77 days
Submission Type
Statement

FLEXMAP 3D

Page Type
Cleared 510(K)
510(k) Number
K133302
510(k) Type
Traditional
Applicant
LUMINEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2014
Days to Decision
77 days
Submission Type
Statement