Clearance Summary
SAF FIXATIVE received FDA 510(k) clearance under submission number K803054, sponsored by Remel Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1980-12-22.
- Submission: K803054
- Applicant / Sponsor: Remel Co.
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class I
- Regulation citation: 21 CFR 864.4010
- Decision date: 1980-12-22
Classification & Regulation
This clearance is catalogued under FDA product code IGB and 21 CFR 864.4010, within the Pathology review panel as a Class I device.