Clearance Summary
WAKO L-TYPE FE, WAKO L-TYPE CALIBRATOR received FDA 510(k) clearance under submission number K984119, sponsored by Wako Chemicals USA, 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 1999-01-15.
- Submission: K984119
- Applicant / Sponsor: Wako Chemicals USA, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1410
- Decision date: 1999-01-15
Classification & Regulation
This clearance is catalogued under FDA product code CFM and 21 CFR 862.1410, within the Clinical Chemistry review panel as a Class I device.