Becton Dickinson Advanced Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Becton Dickinson Advanced Diagnostics - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Becton Dickinson Advanced Diagnostics has 10 FDA 510(k) cleared chemistry devices. Based in Cockeysville, US.
Historical record: 10 cleared submissions from 1991 to 1994.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Becton Dickinson Advanced Diagnostics
10 devices
Cleared
Apr 21, 1994
QTEST(R) STREP
Microbiology
146d
Cleared
Jul 22, 1993
IQ TUPTAKE ASSAY
Chemistry
129d
Cleared
Jul 20, 1993
IQ TT4 ASSAY
Chemistry
127d
Cleared
Mar 18, 1993
PRECISE(TM) HCG(URINE/SERUM) AND PRCISE(TM) PREG
Chemistry
87d
Cleared
Dec 28, 1992
BECTON DICKINSON THYROID STIMULATING HORMONE SYSTE
Chemistry
76d
Cleared
Sep 28, 1992
PRECISE STREP A
Microbiology
68d
Cleared
Sep 15, 1992
IQ IMMUNOCHEMISTRY SISTEM
Chemistry
82d
Cleared
Mar 18, 1992
RIATRAC PLUS
Chemistry
134d
Cleared
Dec 17, 1991
PRECISE TM HCG
Chemistry
28d
Cleared
Dec 16, 1991
PRECISE TM HCG FOR USE IN THE PHYSICIANS OFFICE LA
Chemistry
27d