Clearance Summary
PERCUSSOR received FDA 510(k) clearance under submission number K812166, sponsored by Dhd Medical Products Div. Diemolding Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1981-08-18.
- Submission: K812166
- Applicant / Sponsor: Dhd Medical Products Div. Diemolding Corp.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5665
- Decision date: 1981-08-18
Classification & Regulation
This clearance is catalogued under FDA product code BYI and 21 CFR 868.5665, within the Anesthesiology review panel as a Class II device.