Clearance Summary
NOVATHERM received FDA 510(k) clearance under submission number K851034, sponsored by Medtech Products, 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 1985-09-27.
- Submission: K851034
- Applicant / Sponsor: Medtech Products, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class III
- Regulation citation: 21 CFR 884.2982
- Decision date: 1985-09-27
Classification & Regulation
This clearance is catalogued under FDA product code KXZ and 21 CFR 884.2982, within the Obstetrics/Gynecology review panel as a Class III device.