Supermax Plastic Products Co., Ltd. is one of 18423 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Supermax Plastic Products Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Powder Free Vinyl Patient Examination Gloves (Green), POWDER FREE VINYL PATIENT EXAMINATION GLOVES (YELLOW, WHITE), POWDER FREE VINYL PATIENT EXAMINATION GLOVE
3
Total
3
Cleared
0
Denied
Supermax Plastic Products Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Chino, US.
Historical record: 3 cleared submissions from 2010 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Supermax Plastic Products Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hongray USA Maedical Products, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Supermax Plastic Products Co., Ltd.
3 devices