Hillcrest Biologicals is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hillcrest Biologicals - FDA 510(k) Cleared Devices
33
Total
33
Cleared
0
Denied
Hillcrest Biologicals has 33 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 33 cleared submissions from 1983 to 1992.
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 - Hillcrest Biologicals
33 devices
Cleared
Dec 03, 1992
ARBOVIRUS IGG IFA TEST
Microbiology
478d
Cleared
Dec 03, 1992
ARBOVIRUS IGM IFA TEST
Microbiology
478d
Cleared
Oct 21, 1992
Q FEVER IGG IFA TEST
Microbiology
418d
Cleared
Oct 21, 1992
Q FEVER IGM IFA TEST
Microbiology
154d
Cleared
Jun 28, 1991
LYME DISEASE IGM ELISA
Microbiology
528d
Cleared
Jan 16, 1990
EBV VCA ANTIBODY (IGM)
Microbiology
56d
Cleared
Apr 12, 1989
EBV EARLY ANTIGEN (R+D)
Microbiology
145d
Cleared
Mar 15, 1989
LYME DISEASE IFA (IGM)
Microbiology
190d
Cleared
Jan 24, 1989
EBV-VCA ANTIBODY (IGG)
Microbiology
82d
Cleared
Dec 13, 1988
LYME DISEASE IFA (IGG)
Microbiology
119d
Cleared
May 23, 1988
EBNA ANTIBODY
Microbiology
158d
Cleared
Apr 26, 1988
LYME DISEASE ELISA
Microbiology
82d