K021261Substantially Equivalent
Seednet System and Seednetgold System, Models Gp6t5, Gp5t5, Gp5t3, Hp5t5 & Hp5t3
Galil Medical Ltd., Washington DC / Traditional, Substantially Equivalent
K021261 is the FDA 510(k) clearance record for SEEDNET SYSTEM AND SEEDNETGOLD SYSTEM, MODELS GP6T5, GP5T5, GP5T3, HP5T5 & HP5T3, a class II device, cleared for Galil Medical , Ltd. on under FDA product code GEH (Unit, Cryosurgical, Accessories). FDA records list 31 510(k) clearances for Galil Medical , Ltd., from to . As of , FDA records show one recall naming K021261.
Clearance record
- Decision date
- Received
- (75 days to decision)
- Product code
- GEH Unit, Cryosurgical, Accessories
- Regulation
- 21 CFR 878.4350
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Galil Medical , Ltd. 555 Thirteenth St. NW, Washington DC
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code GEH
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 1 |
| February 2026 | 2 |
| March 2026 | 0 |
| April 2026 | 2 |
| May 2026 | 0 |
| June 2026 | 2 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
