FDA 510(k) Applications Submitted by CALTAG LABORATORIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K990641 02/26/1999 CALTAG FETAL HEMOGLOBIN TEST CALTAG LABORATORIES, INC.
K963954 10/02/1996 CD 19 R-PE, CD19 TRI-COLOR MONOCLONAL ANTIBODY CALTAG LABORATORIES, INC.
K964856 12/04/1996 CD3 FITC/CD19 R-PE/CD45 TRI-COLOR MONOCLONAL ANTIBODY COMBINATION CALTAG LABORATORIES, INC.
K965232 12/31/1996 CALTAG CAL-LYSE CALTAG LABORATORIES, INC.


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