Clearance Summary
CREATININE FOR MANUAL OR AUTOMATED APPLICATIONS received FDA 510(k) clearance under submission number K894389, sponsored by Catachem, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1989-10-12.
- Submission: K894389
- Applicant / Sponsor: Catachem, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.6160
- Decision date: 1989-10-12
Classification & Regulation
This clearance is catalogued under FDA product code GGX and 21 CFR 864.6160, within the Hematology review panel as a Class I device.