Mednet Locator, Inc.
Memphis, TN, US
Mednet Locator, Inc. appears in FDA device records in Memphis, TN. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Mednet Locator, Inc. between 1997 and 2000. The busiest year on record is 1997, with 6. The most recent is 2000, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1997 | 6 |
| 1998 | 1 |
| 2000 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K001406 | HA/GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES | ETA | Substantially Equivalent | |
| K001404 | GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES, GOLD TOTAL WITH FOUNTIAN HEAD, GOLD PISTON | ETA | Substantially Equivalent | |
| K974174 | ULTRABUR | ERL | Substantially Equivalent | |
| K972737 | CAUSSE PISTON | ETB | Substantially Equivalent | |
| K972735 | TOTAL OSSICULAR REPLACEMENT PROSTHESIS (TORP) | ETA | Substantially Equivalent | |
| K972734 | PARTIAL OSSICULAR REPLACEMENT PROSTHESIS (PORP) | ETB | Substantially Equivalent | |
| K972126 | MYRINGOTOMY TUBE | ETD | Substantially Equivalent | |
| K972400 | MYRINGOTOMY TUBE - BOBBIN WITH TAB | ETD | Substantially Equivalent | |
| K971943 | MYRINGOTOMY TUBE | ETD | 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