Clearance Summary
CARDIAC PROBE received FDA 510(k) clearance under submission number K760595, sponsored by G.D. Searle and Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1976-09-17.
- Submission: K760595
- Applicant / Sponsor: G.D. Searle and Co.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1320
- Decision date: 1976-09-17
Classification & Regulation
This clearance is catalogued under FDA product code IZD and 21 CFR 892.1320, within the Radiology review panel as a Class I device.