ClearanceBrief
Company ยท US

Lori Medical Laboratories, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1997. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ESDHearing Aid, Air-Conduction, Prescription7
KHLHearing Aid, Master1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 14, 1997K973376LORI/LORI, LORI-S (LORI STOCK AID)
Lori Medical Laboratories, Inc.
ESD
Aug 15, 1997K972058LORIPRO, LORIPRO II
Lori Medical Laboratories, Inc.
ESD
Jan 8, 1997K964080LORI HEARING AID SIMULATOR
Lori Medical Laboratories, Inc.
KHL
Jul 3, 1995K952711LORI-A
Lori Medical Laboratories, Inc.
ESD
Mar 25, 1994K940639LORI-CIC HEARING AID
Lori Medical Laboratories, Inc.
ESD
Sep 8, 1989K893723LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT
Lori Medical Laboratories, Inc.
ESD
Sep 8, 1989K893722LORI-MODEL H, HALF CONCHA IN-THE-EAR INSTRUMENT
Lori Medical Laboratories, Inc.
ESD
Sep 8, 1989K893721LORI-MODEL O, LOW PROFILE IN-THE EAR INSTRUMENT
Lori Medical Laboratories, Inc.
ESD

Latest recalls

DateFirm and productCodeLinked 510(k)
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