Boots-Celltech Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Boots-Celltech Diagnostics, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Boots-Celltech Diagnostics, Inc. has 20 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 20 cleared submissions from 1984 to 1989. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Boots-Celltech Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Boots-Celltech Diagnostics, Inc.
20 devices
Cleared
Nov 17, 1989
IDEIA HERPES SIMPLEX VIRUS TEST
Microbiology
918d
Cleared
Dec 08, 1988
MODIFIED IDEIA CHLAMYDIA TEST
Microbiology
283d
Cleared
Apr 18, 1988
SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY
Chemistry
53d
Cleared
Mar 24, 1988
CHEMELIA FREE THYROXINE(FT4)/ENZYME IMMUNO. (EIA)
Chemistry
118d
Cleared
Feb 24, 1988
IMAGEN INFLUENZA VIRUS A AND B TESTMI
Microbiology
210d
Cleared
Feb 02, 1988
OVEIA (TM) DUAL ANALYTE
Chemistry
197d
Cleared
Oct 20, 1987
CHEMELIA ENZYME IMMUNOASSAY FOR (TSH)
Chemistry
42d
Cleared
Jun 15, 1987
MODIFIED (DIRECTIONS FOR USE) FOR IDEIA(TM) TEST
Microbiology
18d
Cleared
May 08, 1987
IMAGEN HERPES SIMPLEX VIRUS (HSV) TYPING TEST
Microbiology
86d
Cleared
Apr 20, 1987
IDEIA(TM) CHLAMYDIA SPECIMEN COLLECTION KIT
Microbiology
119d
Cleared
Mar 12, 1987
MODIFIED IMAGEN(TM) CHLAMYDIA TEST
Microbiology
113d
Cleared
Aug 19, 1986
MODIFIED IDEIA CHLAMYDIA TEST
Microbiology
91d