Clearance Summary
NEO-FLOAT NEONATAL FLOTATION SYS & RHYT received FDA 510(k) clearance under submission number K832829, sponsored by Clinical Data Instruments, 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 1983-10-04.
- Submission: K832829
- Applicant / Sponsor: Clinical Data Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5170
- Decision date: 1983-10-04
Classification & Regulation
This clearance is catalogued under FDA product code IOQ and 21 CFR 890.5170, within the Physical Medicine review panel as a Class II device.