Ningbo Kaida Rubber and Plastic Technology Co., LT is one of 2194 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Ningbo Kaida Rubber and Plastic Technology Co., LT - FDA 510(k) Clear...
Recent clearances: CONTACT LENS CASE
1
Total
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Cleared
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Denied
Ningbo Kaida Rubber and Plastic Technology Co., LT has 1 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Ningbo Kaida Rubber and Plastic Technology Co., LT Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ningbo Kaida Rubber and Plastic Technology Co., LT
1 devices