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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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