Lori Medical Laboratories, Inc.
Long Lake, MN, US
Lori Medical Laboratories, Inc. appears in FDA device records in Long Lake, MN. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Lori Medical Laboratories, Inc. between 1989 and 1997. The busiest year on record is 1989, with 3. The most recent is 1997, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 3 |
| 1994 | 1 |
| 1995 | 1 |
| 1997 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K973376 | LORI/LORI, LORI-S (LORI STOCK AID) | ESD | Substantially Equivalent | |
| K972058 | LORIPRO, LORIPRO II | ESD | Substantially Equivalent | |
| K964080 | LORI HEARING AID SIMULATOR | KHL | Substantially Equivalent | |
| K952711 | LORI-A | ESD | Substantially Equivalent | |
| K940639 | LORI-CIC HEARING AID | ESD | Substantially Equivalent | |
| K893723 | LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT | ESD | Substantially Equivalent | |
| K893722 | LORI-MODEL H, HALF CONCHA IN-THE-EAR INSTRUMENT | ESD | Substantially Equivalent | |
| K893721 | LORI-MODEL O, LOW PROFILE IN-THE EAR INSTRUMENT | ESD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain