Caltag Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Caltag Laboratories, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Caltag Laboratories, Inc. has 12 FDA 510(k) cleared hematology devices. Based in South San Francisco, US.
Historical record: 12 cleared submissions from 1995 to 1999.
Browse the complete list of FDA 510(k) cleared hematology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Caltag Laboratories, Inc.
12 devices
Cleared
Sep 17, 1999
CALTAG FETAL HEMOGLOBIN TEST
Hematology
203d
Cleared
May 14, 1997
CALTAG CAL-LYSE
Hematology
134d
Cleared
Jan 17, 1997
CD3 FITC/CD19 R-PE/CD45 TRI-COLOR MONOCLONAL ANTIBODY COMBINATION
Hematology
44d
Cleared
Nov 25, 1996
CD 19 R-PE, CD19 TRI-COLOR MONOCLONAL ANTIBODY
Hematology
54d
Cleared
Dec 21, 1995
CD3 FITC/CD8 R-PE MONOCLONAL ANTIBODY COMBINATION
Hematology
295d
Cleared
Dec 21, 1995
CD3 FITC/CD8 R-PE/CD45 TRI-COLOR MONOCLONAL ANTIBODY COMBINATION
Hematology
295d
Cleared
Dec 21, 1995
CD3 FITC/CD4 R-PE MONOCLONAL ANTIBODY COMBINATION
Hematology
295d
Cleared
Dec 21, 1995
CD3 TRI-COLOR/CD4 R-PE/CD8 FITC MONOCLONAL ANTIBODY COMBINATION
Hematology
288d
Cleared
Dec 20, 1995
CD3 FITC/CD4 R-PE/CD45 TRI-COLOR MONOCLONAL ANTIBODY COMBINATION
Hematology
294d
Cleared
Jun 20, 1995
CALTAG CD8 FITC AND CD8 R-PE MONOCLONAL ANTIBODIES
Hematology
301d
Cleared
Jun 20, 1995
CALTAG CD3 FITC, R-PE, TRI-COLOR MONOCLONAL ANTIBODY
Hematology
301d
Cleared
Jun 20, 1995
CALTAG CD4 R-PE MONOCLONAL ANTIBODY
Hematology
301d