Clearance Summary
MODIFIED SITE PERISTALTIC FOOTSWITCH received FDA 510(k) clearance under submission number K905620, sponsored by Site Microsurgical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-02-27.
- Submission: K905620
- Applicant / Sponsor: Site Microsurgical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 1991-02-27
Classification & Regulation
This clearance is catalogued under FDA product code EBW and 21 CFR 872.4200, within the Dental review panel as a Class I device.