Clearance Summary
SKALPI 3200 received FDA 510(k) clearance under submission number K946382, sponsored by Wiscco Development, Inc.. 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 1995-05-30.
- Submission: K946382
- Applicant / Sponsor: Wiscco Development, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5975
- Decision date: 1995-05-30
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.