Guangzhou Improve Medical Instruments Co., Ltd.
Guangzhou Improve Medical Instruments Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2016, with 3 FDA device recalls on record.
Top product codes for Guangzhou Improve Medical Instruments Co., Ltd.
FDA recalls by Guangzhou Improve Medical Instruments Co., Ltd.
- Z-2549-2018 — Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
- Z-1217-2019 — Prevent G Safety Winged Blood Collection Set Glide - Rx Only -Sterile/EO - Product Usage: The IMPROSAFE Blood Collection Set is single-use, sterile, winged needle bonded to a flexible tubing with luer adapter. The needle consists of (1) a winged needle, (2) a flexible tubing, (3) a luer adaptor. (4) a safety shield, The products and evacuated blood collection tube/ syringe are used together for the collection of venous blood.
- Z-2790-2018 — Improve Blood Collection Sets with Multiple Sample Luer Adapter - Sterile/EO Product Usage: The Blood Collection Set are single-use, sterile, winged needle bonded to a flexible tubing with luer adapter. The needle consists of (1) a winged needle, (2) a flexible tubing, (3) a luer adaptor. The products and evacuated blood collection tube/ syringe are used together for the collection of venous blood.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Guangzhou Improve Medical Instruments Co., Ltd.
- K153388 — IMPROSAFE Blood Collection Set with Pre-attached Holder, IMPROVACUTER Blood Collection Set Pre-attached Holder, IMPROSAFE Blood Collection Set, IMPROVACUTER Blood Collection Set, IMPROSAFE Multi Sample Needle, IMPROSAFE Multi Sample Needle (Flashback), IMPROVACUTER Multi Sample Needle
- K093910 — IMPROVACUTER GEL & CLOT ACTIVATOR TUBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.