Clearance Summary
SITZ BATH, SINGLE PATIENT USE #8100 received FDA 510(k) clearance under submission number K831762, sponsored by Lsl Industries, 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 1983-06-24.
- Submission: K831762
- Applicant / Sponsor: Lsl Industries, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5125
- Decision date: 1983-06-24
Classification & Regulation
This clearance is catalogued under FDA product code KTC and 21 CFR 890.5125, within the Physical Medicine review panel as a Class I device.