Bioclinical Systems, Inc.
Bioclinical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1995.
Top product codes for Bioclinical Systems, Inc.
Recent clearances by Bioclinical Systems, Inc.
- K950196 — CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIA
- K945911 — CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARS
- K933122 — MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGAR
- K933121 — MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGAR
- K873086 — ROUND 1
- K860333 — MICRO-ELISA HLH TEST KIT MONOCLONAL
- K860334 — VISI-CHECK HLH TEST MONOCLONAL
- K855227 — MICRO-EIA THEOPHYLLINE TEST KIT MONOCLONAL
- K854059 — MICRO-ELISA HCG EST KIT VISI-CHECK HCG TEST KIT NO
- K854379 — MICRO-ELISA TSH TEST KIT-VISI-CHECK TSH TEST KIT
- K850079 — NOW HOME PREGN. TEST KIT ENZYME IMMUNOASSAY HCG
- K850257 — BCS GLUCOSE COLORIMETRIC TEST
- K850258 — BCS POTASSIUM TURBIDIMETRIC TEST
Data sourced from openFDA. This site is unofficial and independent of the FDA.