Clearance Summary
REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S received FDA 510(k) clearance under submission number K931484, sponsored by Portable Power Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1994-02-17.
- Submission: K931484
- Applicant / Sponsor: Portable Power Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 1994-02-17
Classification & Regulation
This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.