Clearance Summary
NORELCO VIBRATING BOARD V900 received FDA 510(k) clearance under submission number K830715, sponsored by North American Philips Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1983-05-25.
- Submission: K830715
- Applicant / Sponsor: North American Philips Corp.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5975
- Decision date: 1983-05-25
Classification & Regulation
This clearance is catalogued under FDA product code IRO and 21 CFR 890.5975, within the Physical Medicine review panel as a Class I device.