Clearance Summary
BABY POD received FDA 510(k) clearance under submission number K030283, sponsored by Prism Enterprises, 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 2003-04-22.
- Submission: K030283
- Applicant / Sponsor: Prism Enterprises, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6900
- Decision date: 2003-04-22
Classification & Regulation
This clearance is catalogued under FDA product code FPP and 21 CFR 880.6900, within the General Hospital review panel as a Class I device.