Clearance Summary
KAYE SCOOT-ABOUT, MODEL SB1 received FDA 510(k) clearance under submission number K924848, sponsored by Kaye Products, 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 1993-02-12.
- Submission: K924848
- Applicant / Sponsor: Kaye Products, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3100
- Decision date: 1993-02-12
Classification & Regulation
This clearance is catalogued under FDA product code INM and 21 CFR 890.3100, within the Physical Medicine review panel as a Class I device.