Clearance Summary
ELECTRONIC DEPILATORY MODEL 303 received FDA 510(k) clearance under submission number K770187, sponsored by Electronic Depilatory, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1977-02-23.
- Submission: K770187
- Applicant / Sponsor: Electronic Depilatory, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.5360
- Decision date: 1977-02-23
Classification & Regulation
This clearance is catalogued under FDA product code KCX and 21 CFR 878.5360, within the General, Plastic Surgery review panel as a Class I device.