Clearance Summary
TRANSWORLD 360V, MODEL A1-4040 received FDA 510(k) clearance under submission number K872357, sponsored by Transworld X-Ray Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1987-07-15.
- Submission: K872357
- Applicant / Sponsor: Transworld X-Ray Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1700
- Decision date: 1987-07-15
Classification & Regulation
This clearance is catalogued under FDA product code IZO and 21 CFR 892.1700, within the Radiology review panel as a Class I device.