Clearance Summary
MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE received FDA 510(k) clearance under submission number K960549, sponsored by Neward Enterprises, 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 1996-08-29.
- Submission: K960549
- Applicant / Sponsor: Neward Enterprises, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4340
- Decision date: 1996-08-29
Classification & Regulation
This clearance is catalogued under FDA product code HDB and 21 CFR 884.4340, within the Obstetrics/Gynecology review panel as a Class II device.