Kawasumi Laboratories Co., Ltd.
Kawasumi Laboratories Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2000.
Top product codes for Kawasumi Laboratories Co., Ltd.
Recent clearances by Kawasumi Laboratories Co., Ltd.
- K994323 — KAWASUMI LABORATORIES PHILEBOTOMY SET
- K974829 — NON-PVC FLUID PATH PORT ACCESS INFUSION SET (WITH AND WITHOUT INJECTION SET)
- K964117 — NON-PVC FLUID PATH PORT ACCESS INFUSION SET WITH SLIT SEPTUM INJECTION SITE
- K935514 — VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER
- K935505 — WINGED COLLECTION SET W/MULTI-SAMPLE LUER ADAPTER
- K935506 — MULTI-SAMPLE LUER ADAPTER FOR BLOOD SAMPLE COLLECTION
- K930012 — KAWASUMI LABORATORIES K-CUFF
- K921901 — PORT ACCESS INFUSION SET
- K921902 — PORT ACCESS NEEDLE
- K923323 — INTERMITTENT INJECTION SITE
- K896892 — KAWASUMI Y-TYPE BLOOD ADMINISTRATION SET
- K896893 — KAWASUMI I.V. ADMINISTRATION SET WITH BURETTE
- K896894 — KAWASUMI BLOOD ADMINISTRATION SET
- K896895 — KAWASUMI I.V. ADMINISTRATION SET
- K896896 — KAWASUMI SMALL VEIN INFUSION SET
- K883748 — RENAK-E & RENEK-A SERIES HOLLOW FIBER DIALYZERS
- K873421 — KAWASUMI A.V. FISTULA SET
- K873516 — KAWASUMI BLOOD TUBING LINE
Data sourced from openFDA. This site is unofficial and independent of the FDA.