Clearance Summary
TUBE GRIP received FDA 510(k) clearance under submission number K922404, sponsored by Georgia Medical Products, 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 1992-11-23.
- Submission: K922404
- Applicant / Sponsor: Georgia Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.4200
- Decision date: 1992-11-23
Classification & Regulation
This clearance is catalogued under FDA product code KRI and 21 CFR 870.4200, within the Cardiovascular review panel as a Class I device.