Clearance Summary
SORVALL EMBEDDING MEDIUM received FDA 510(k) clearance under submission number K760602, sponsored by E.I. Dupont DE Nemours & Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1976-09-21.
- Submission: K760602
- Applicant / Sponsor: E.I. Dupont DE Nemours & Co., Inc.
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class I
- Regulation citation: 21 CFR 864.4010
- Decision date: 1976-09-21
Classification & Regulation
This clearance is catalogued under FDA product code KEO and 21 CFR 864.4010, within the Pathology review panel as a Class I device.