FDA applicant
Suzhou Weikang Medical Apparatus Co., Ltd.
FDA records 2 decisions for Suzhou Weikang Medical Apparatus Co., Ltd. (Guangzhou, Guangdong, CN) from 2014 to 2015: 2 510(k) clearances. Most are in product codes BTR (Tube, Tracheal (W/Wo Connector)) and CAF (Nebulizer (Direct Patient Interface)). Its devices cite 4 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Suzhou Weikang Medical Apparatus Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2015
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2014.
Planning a device like Suzhou Weikang Medical Apparatus Co.…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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