Clearance Summary
HH SUBCUTANEOUS ACCESS PORT received FDA 510(k) clearance under submission number K833672, sponsored by Holter-Hausner Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1984-03-06.
- Submission: K833672
- Applicant / Sponsor: Holter-Hausner Intl.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5550
- Decision date: 1984-03-06
Classification & Regulation
This clearance is catalogued under FDA product code LKG and 21 CFR 882.5550, within the Neurology review panel as a Class II device.