Clearance Summary
LIBERTY HOT PACK AND LIBERTY KOLD PACK received FDA 510(k) clearance under submission number K902839, sponsored by Liberty Ent.. 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 1990-07-25.
- Submission: K902839
- Applicant / Sponsor: Liberty Ent.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5710
- Decision date: 1990-07-25
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.