Clearance Summary
TIPSTOP(TM) received FDA 510(k) clearance under submission number K896068, sponsored by Gambro-Hospal, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1990-09-10.
- Submission: K896068
- Applicant / Sponsor: Gambro-Hospal, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5240
- Decision date: 1990-09-10
Classification & Regulation
This clearance is catalogued under FDA product code KGX and 21 CFR 880.5240, within the General Hospital review panel as a Class I device.