Medical Device Manufacturer · US , Long Lake , MN

Lori Medical Laboratories, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1989
8
Total
8
Cleared
0
Denied

Lori Medical Laboratories, Inc. has 8 FDA 510(k) cleared medical devices. Based in Long Lake, US.

Historical record: 8 cleared submissions from 1989 to 1997. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Lori Medical Laboratories, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lori Medical Laboratories, Inc.

8 devices
1-8 of 8
Cleared Oct 14, 1997
LORI/LORI, LORI-S (LORI STOCK AID)
K973376 · ESD
Ear, Nose, Throat · 36d
Cleared Aug 15, 1997
LORIPRO, LORIPRO II
K972058 · ESD
Ear, Nose, Throat · 74d
Cleared Jan 08, 1997
LORI HEARING AID SIMULATOR
K964080 · KHL
Ear, Nose, Throat · 89d
Cleared Jul 03, 1995
LORI-A
K952711 · ESD
Ear, Nose, Throat · 19d
Cleared Mar 25, 1994
LORI-CIC HEARING AID
K940639 · ESD
Ear, Nose, Throat · 39d
Cleared Sep 08, 1989
LORI-MODEL O, LOW PROFILE IN-THE EAR INSTRUMENT
K893721 · ESD
Ear, Nose, Throat · 114d
Cleared Sep 08, 1989
LORI-MODEL H, HALF CONCHA IN-THE-EAR INSTRUMENT
K893722 · ESD
Ear, Nose, Throat · 114d
Cleared Sep 08, 1989
LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT
K893723 · ESD
Ear, Nose, Throat · 114d
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