Clearance Summary
JAKOBI SURG. INSTR- #11 38/39/45/46/67 received FDA 510(k) clearance under submission number K834197, sponsored by Imm Enterprises , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1984-01-27.
- Submission: K834197
- Applicant / Sponsor: Imm Enterprises , Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1984-01-27
Classification & Regulation
This clearance is catalogued under FDA product code EMF and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.