Clearance Summary
PM3000 & PM3100 VACUUM REGULATOR received FDA 510(k) clearance under submission number K922817, sponsored by Precision Medical, 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 1993-03-04.
- Submission: K922817
- Applicant / Sponsor: Precision Medical, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6740
- Decision date: 1993-03-04
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.