Microbix Biosystems, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Microbix Biosystems, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Microbix Biosystems, Inc. has 7 FDA 510(k) cleared medical devices. Based in Canada, CA.
Historical record: 7 cleared submissions from 1985 to 1989. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Microbix Biosystems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Microbix Biosystems, Inc.
7 devices
Cleared
Oct 16, 1989
TOXOPLASMA GONDII-CF ANTIGEN AND CONTROL ANTIGEN
Microbiology
117d
Cleared
Oct 16, 1989
RUBELLA ANTIGEN AND CONTROL ANTIGEN
Microbiology
117d
Cleared
Nov 12, 1985
CMV-COMPLEMENT FIXATION ANTIGEN AND NEGATIVE CONTR
Microbiology
126d
Cleared
Nov 12, 1985
VARICELLA-ZOSTER-COMPLE FIX ANTIGEN AND NEG CONTRO
Microbiology
126d
Cleared
Nov 12, 1985
HERPES HOMINUS I-COMPLE FIX ANTIGEN & NEGATIVE CLT
Microbiology
126d
Cleared
Nov 12, 1985
MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT
Immunology
126d
Cleared
Aug 01, 1985
MYCOPLASMA SPP SEROLOGICAL REAGENTS
Microbiology
23d