Kronos Electrocautery Device
Single Pass, Inc.
SINGLE PASS, INC.
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3025268689 | 3025268689 | SINGLE PASS, INC. | 1 | N | 2027-01-01 | 105 North Pointe Drive Suite B Lake Forest CA US 92630 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 311794 | 1339714941 | K262720 | SP Electrocautery Device (SP18 Max);SP Electrocautery Device (SP20 Max) | GEI | 2026-10-26 |
| 311794 | 1309770078 | K232805 | Kronos Electrocautery Device | GEI | 2024-04-25 |
| 311794 | 1944216746 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| GEI | 2 | 2026-10-26 |