Clearance Summary
VACUUM REGULATOR 0-2000 MMHG VR-1000 received FDA 510(k) clearance under submission number K834224, sponsored by Trimeter Instrument Corp.. 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 1984-02-27.
- Submission: K834224
- Applicant / Sponsor: Trimeter Instrument Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6740
- Decision date: 1984-02-27
Classification & Regulation
This clearance is catalogued under FDA product code KDP and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.