Clearance Summary
ENDOCYTE TM received FDA 510(k) clearance under submission number K944238, sponsored by D.L. Nelson and Assoc., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1995-09-15.
- Submission: K944238
- Applicant / Sponsor: D.L. Nelson and Assoc., Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.4530
- Decision date: 1995-09-15
Classification & Regulation
This clearance is catalogued under FDA product code HCY and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class I device.