Clearance Summary
SIMUTANEOUS FIXATION & DECALCIFYING SOLUTION CAL-E received FDA 510(k) clearance under submission number K850636, sponsored by Fisher Scientific Co., LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1985-03-20.
- Submission: K850636
- Applicant / Sponsor: Fisher Scientific Co., LLC
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class I
- Regulation citation: 21 CFR 864.4010
- Decision date: 1985-03-20
Classification & Regulation
This clearance is catalogued under FDA product code KDX and 21 CFR 864.4010, within the Pathology review panel as a Class I device.