Medical Device Manufacturer · US , Tucson , AZ

Je Liss & Co., Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Je Liss & Co., Inc. has 1 FDA 510(k) cleared medical devices. Based in Tucson, US.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Je Liss & Co., Inc. Filter by specialty or product code using the sidebar.

Je Liss & Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Je Liss & Co., Inc.

1 devices

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