New Horizons Diagnostics Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
New Horizons Diagnostics Co. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
New Horizons Diagnostics Co. has 10 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1982 to 1995.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - New Horizons Diagnostics Co.
10 devices
Cleared
Jun 27, 1995
CHOLERA SMART(TM)
Microbiology
756d
Cleared
Mar 23, 1993
PYLORISCREEN
Microbiology
160d
Cleared
Dec 07, 1992
CHOLERASCREEN
Microbiology
199d
Cleared
Feb 19, 1988
RAPID COLORIMETRIC DIRECT STREP A TEST
Microbiology
92d
Cleared
May 28, 1987
SYPHILIS SEROLOGICAL REAGENTS
Microbiology
62d
Cleared
May 13, 1987
THE GONOGEN II TEST KIT FOR NEISSERIA GONORRHOEAE
Microbiology
55d
Cleared
Jun 30, 1986
RAPID BACTERIURIA SCREEN (RBS)
Microbiology
21d
Cleared
Jul 05, 1985
LATEX AGGLUTINATION TEST
Microbiology
106d
Cleared
Aug 04, 1982
IMPROVED GONO GEN
Microbiology
89d
Cleared
Jan 29, 1982
NEISSERIA GONORRHOEAE TEST
Microbiology
25d