Clearance Summary
OSMOMETER MODEL 2400 received FDA 510(k) clearance under submission number K911092, sponsored by Advanced Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1991-05-22.
- Submission: K911092
- Applicant / Sponsor: Advanced Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2730
- Decision date: 1991-05-22
Classification & Regulation
This clearance is catalogued under FDA product code JJM and 21 CFR 862.2730, within the Clinical Chemistry review panel as a Class I device.