Clearance Summary
NEO NEST received FDA 510(k) clearance under submission number K112547, sponsored by Denovo Proucts, LLC. 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 2012-03-06.
- Submission: K112547
- Applicant / Sponsor: Denovo Proucts, LLC
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5710
- Decision date: 2012-03-06
Classification & Regulation
This clearance is catalogued under FDA product code IMD and 21 CFR 890.5710, within the Physical Medicine review panel as a Class I device.