Clearance Summary
SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND received FDA 510(k) clearance under submission number K932265, sponsored by Symbiosis 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 1993-08-09.
- Submission: K932265
- Applicant / Sponsor: Symbiosis Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.1075
- Decision date: 1993-08-09
Classification & Regulation
This clearance is catalogued under FDA product code FCL and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class I device.