Clearance Summary
HEYER-SCHULTE DISPOSABLE PERITONEAL CATHETER PASSE received FDA 510(k) clearance under submission number K895868, sponsored by Baxter Healthcare Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1989-10-31.
- Submission: K895868
- Applicant / Sponsor: Baxter Healthcare Corp
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class I
- Regulation citation: 21 CFR 882.4545
- Decision date: 1989-10-31
Classification & Regulation
This clearance is catalogued under FDA product code GYK and 21 CFR 882.4545, within the Neurology review panel as a Class I device.