Kawasumi Laboratories Co., Ltd.
FDA 510(k) medical device clearances.
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.