Bion Ent., Ltd.
Bion Ent., Ltd. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1993.
Top product codes for Bion Ent., Ltd.
Recent clearances by Bion Ent., Ltd.
- K926066 — BION MUMPS-G ANTIBODY TEST SYSTEM
- K901054 — BION BORRELIA BURGDORFERI ANTIGEN SUBSTRATE SLIDE
- K894622 — VARICELLA ZOSTER VIRUS
- K894623 — RESPIRATORY SYNCYTIAL VIRUS
- K894624 — MUMPS VIRUS
- K894626 — EPSTEIN-BARR VIRUS-NUCLEAR ANTIGEN
- K891785 — BION EBV-G (VCA) TEST SYSTEM
- K894625 — CHLAMYDIA (LGV-1)
- K893240 — BION EBV-M (VCA) TEST SYSTEM
- K890616 — BION DIRECT IDENTIFICATION CONTROL SLIDE
- K881261 — BION HSV1-G OR HSV2-G TEST SYSTEM
- K880679 — BION CMV-G TEST SYSTEM
- K872845 — BION ANTINUCLEAR ANTIBODY(ANA)TEST KIT/CONTR SERUM
- K800434 — PORTABLE MEDICAL ULTRASOUND SCANNER
Data sourced from openFDA. This site is unofficial and independent of the FDA.