Clearance Summary
CMI VACUUM PUMP W/#101A VACUUM PUMP (AUTO-CLAVE.) received FDA 510(k) clearance under submission number K895446, sponsored by Challenge Mfg., 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 1989-11-27.
- Submission: K895446
- Applicant / Sponsor: Challenge Mfg., Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4340
- Decision date: 1989-11-27
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.