Clearance Summary
JACKSON ESOPHAGEAL BOUGIE, X-RAY OPAQUE received FDA 510(k) clearance under submission number K800623, sponsored by Pilling Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1980-04-24.
- Submission: K800623
- Applicant / Sponsor: Pilling Co.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4420
- Decision date: 1980-04-24
Classification & Regulation
This clearance is catalogued under FDA product code KCD and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.