Clearance Summary
Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/Divider received FDA 510(k) clearance under submission number K182588, sponsored by Surgical Instrument Service and Savings Inc.(Dba Medline Ren. 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 2018-10-31.
- Submission: K182588
- Applicant / Sponsor: Surgical Instrument Service and Savings Inc.(Dba Medline Ren
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2018-10-31
Classification & Regulation
This clearance is catalogued under FDA product code NUJ and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.