Clearance Summary
The ZIP Accessory Shuttle for PleuraFlow System received FDA 510(k) clearance under submission number K191733, sponsored by Clearflow, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2019-07-26.
- Submission: K191733
- Applicant / Sponsor: Clearflow, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4780
- Decision date: 2019-07-26
Classification & Regulation
This clearance is catalogued under FDA product code OTK and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.