Clearance Summary
DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS received FDA 510(k) clearance under submission number K881841, sponsored by Buckman Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-12-13.
- Submission: K881841
- Applicant / Sponsor: Buckman Co., Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2770
- Decision date: 1988-12-13
Classification & Regulation
This clearance is catalogued under FDA product code DSB and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.