Clearance Summary
Otsuka Digital Feedback Device-RW received FDA 510(k) clearance under submission number K223463, sponsored by Otsuka America Pharmaceutical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2023-08-11.
- Submission: K223463
- Applicant / Sponsor: Otsuka America Pharmaceutical, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6305
- Decision date: 2023-08-11
Classification & Regulation
This clearance is catalogued under FDA product code OZW and 21 CFR 880.6305, within the General Hospital review panel as a Class II device.