Clearance Summary
LAPAROOPTX(TM) INTRAOPER DEFLECT CHOLEDOCHOSCOPE received FDA 510(k) clearance under submission number K912839, sponsored by Baxter Healthcare Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1991-09-25.
- Submission: K912839
- Applicant / Sponsor: Baxter Healthcare Corp
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5520
- Decision date: 1991-09-25
Classification & Regulation
This clearance is catalogued under FDA product code FBW and 21 CFR 876.5520, within the Gastroenterology, Urology review panel as a Class I device.