Medical Device Manufacturer · US , Tucson , AZ

Je Liss & Co., Inc.

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Je Liss & Co., Inc. — FDA 510(k) Submissions

Je Liss & Co., Inc. has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Assistive Listening . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

HEARIT

K934805 · LZI Device, Assistive Listening · Ear, Nose, Throat

Feb 1994 123d

Je Liss & Co., Inc.

Je Liss & Co., Inc. — FDA 510(k) Submissions

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