Industrias Palex C/O Dma Med-Chem Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Industrias Palex C/O Dma Med-Chem Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Industrias Palex C/O Dma Med-Chem Corp. has 5 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 5 cleared submissions from 1987 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Industrias Palex C/O Dma Med-Chem Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Industrias Palex C/O Dma Med-Chem Corp.
5 devices
Cleared
Mar 07, 1994
EPISENSOR PLUS
General Hospital
747d
Cleared
Mar 26, 1992
ULCUFLEX HYDROCOLOID POWDER
General & Plastic Surgery
58d
Cleared
Mar 26, 1992
ULCUFLEX HYDROCULLOID DRESSING
General & Plastic Surgery
58d
Cleared
Mar 26, 1992
ULCUFLEX HYDROCOLLOID PASTE
General & Plastic Surgery
58d
Cleared
Jul 08, 1987
PALEX (R) OSTOMY
Gastroenterology & Urology
72d