Clearance Summary
FSH RIA KIT (125I) received FDA 510(k) clearance under submission number K772188, sponsored by Diagnostic Products Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1977-12-22.
- Submission: K772188
- Applicant / Sponsor: Diagnostic Products Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1977-12-22
Classification & Regulation
This clearance is catalogued under FDA product code FSH and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.