Clearance Summary
OMNI WARM GEL PACKS received FDA 510(k) clearance under submission number K936084, sponsored by Omni Therm, Inc.. 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 1994-03-31.
- Submission: K936084
- Applicant / Sponsor: Omni Therm, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5710
- Decision date: 1994-03-31
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.