GEJ — Carrier, Ligature Class I
FDA Device Classification
Classification Details
- Product Code
- GEJ
- Device Class
- Class I
- Regulation Number
- 878.4800
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K240185 | cypris medical | Cypris eXact Suture Placement Device | May 3, 2024 |
| K900958 | solos endoscopy | GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM | April 18, 1990 |
| K900959 | solos endoscopy | GS-1400 TOOTHED DISSECTING FORCEP, 5MM, INSULATED | April 18, 1990 |
| K884553 | cook ob/gyn | STAMEY NEEDLE | November 14, 1988 |
| K874342 | cox-uphuff intl | LIGATURE CARRIER/PACKER, HYDROXYLAPATITE | November 13, 1987 |