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LUMINEX FLEXMAP 3D INSTRUMENT SYSTEM, LUMINEX XPONENT 4.0 SPI SOFTWARE, FLEXMAP 3D IVD CALIBRATION KIT, FLEXMAP 3D IVD P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121399
510(k) Type
Traditional
Applicant
LUMINEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2013
Days to Decision
245 days
Submission Type
Statement

LUMINEX FLEXMAP 3D INSTRUMENT SYSTEM, LUMINEX XPONENT 4.0 SPI SOFTWARE, FLEXMAP 3D IVD CALIBRATION KIT, FLEXMAP 3D IVD P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121399
510(k) Type
Traditional
Applicant
LUMINEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2013
Days to Decision
245 days
Submission Type
Statement