Clearance Summary
BILICHEK NON-INVASIVE BILIRUBIN ANALYZER received FDA 510(k) clearance under submission number K994438, sponsored by Spectrx, 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 2000-02-04.
- Submission: K994438
- Applicant / Sponsor: Spectrx, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1113
- Decision date: 2000-02-04
Classification & Regulation
This clearance is catalogued under FDA product code MQM and 21 CFR 862.1113, within the Clinical Chemistry review panel as a Class I device.