Clearance Summary
PLEURAL DRAINAGE SYSTEM #PDS-4300 received FDA 510(k) clearance under submission number K812224, sponsored by Bentley Laboratories, 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 1981-09-09.
- Submission: K812224
- Applicant / Sponsor: Bentley Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6740
- Decision date: 1981-09-09
Classification & Regulation
This clearance is catalogued under FDA product code KDQ and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.