Clearance Summary
GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS received FDA 510(k) clearance under submission number K873248, sponsored by Medical Engineering Laboratory, Inc.. 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 1987-12-30.
- Submission: K873248
- Applicant / Sponsor: Medical Engineering Laboratory, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1987-12-30
Classification & Regulation
This clearance is catalogued under FDA product code OCZ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.