Clearance Summary
POWRPAK REPLACEMENT BATTERIES FOR PHISIO-CONTROL LIFEPAK 5/10 received FDA 510(k) clearance under submission number K934067, sponsored by National Custom Ent., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1993-10-07.
- Submission: K934067
- Applicant / Sponsor: National Custom Ent., Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.5300
- Decision date: 1993-10-07
Classification & Regulation
This clearance is catalogued under FDA product code DRK and 21 CFR 870.5300, within the Cardiovascular review panel as a Class III device.