Clearance Summary
MYOGLOBIN ELISA TEST KIT received FDA 510(k) clearance under submission number K923195, sponsored by Immuno Diagnostic Center, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1992-11-06.
- Submission: K923195
- Applicant / Sponsor: Immuno Diagnostic Center, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5680
- Decision date: 1992-11-06
Classification & Regulation
This clearance is catalogued under FDA product code DDR and 21 CFR 866.5680, within the Immunology review panel as a Class II device.