Lead-Lok, Inc.
Sandpoint, ID, US
Lead-Lok, Inc. appears in FDA device records in Sandpoint, ID. FDA records list 5 510(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
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Lead-Lok, Inc. between 1989 and 2001. The busiest year on record is 1992, with 2. The most recent is 2001, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 1 |
| 1990 | 1 |
| 1992 | 2 |
| 2001 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K010431 | LEAD-LOK REUSABLE TENS/ NMES ELECTRODES | GXY | Substantially Equivalent | |
| K911529 | BUNNY ELECTRODE/STEALTH ELECTRODE PRE WIRED EEG | DRX | Substantially Equivalent | |
| K911518 | BUNNY ELECTRODE/STEALTH SOLID GEL-SNAP ON FOAM | DRX | Substantially Equivalent | |
| K903729 | GOLD GATORS | DRY | Substantially Equivalent | |
| K895100 | ECHO GEL (RAINFOREST) | ITX | 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