NIKKISO CO., LTD.
NIKKISO CO., LTD. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2025.
Top product codes for NIKKISO CO., LTD.
Recent clearances by NIKKISO CO., LTD.
- K242155 — DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO)
- K242176 — BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series (AL-ADC-E(U), AL-CDC-E(U), C18RDC-E(U), C18BDD-E(U), C18SFD-E(U)
- K242479 — BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series AL-ADC-PU, AL-CDC-PU, C18RDC-PU, C18BDD-PU, C18SFD-PU
- K231589 — Blood Tubing Lines for Hemodialysis AV06C-E
- K230514 — Blood Tubing Lines for Hemodialysis AL Series (Archloop), Blood Tubing Lines for Hemodialysis C18 Series
- K152938 — DBB-06 Hemodialysis Delivery System
- K091978 — DBB-06 HEMODIALYSIS DELIVERY SYSTEM
- K082719 — NIKKLINE BLOOD TUBING LINES WITH TRANSDUCER PROTECTORS, MODELS AV06A-P, AVO6B-P, AV06C-P
- K061519 — MODIFICATION TO DBB-05 HEMODIALYSIS DELIVERY SYSTEM
- K953996 — NIKKISO CO, LTD., FLX10GW, 12GW, 15GW, 18GW & 21GW HEMODIALYZERS
- K803068 — NIKKISO ND-14 PARALLEL FLOW DIALYZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.