Clearance Summary
ISCOVE'S MODIFIED DULBECCO'S MEDIUM (IMDM) received FDA 510(k) clearance under submission number K873022, sponsored by J R Scientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1987-08-19.
- Submission: K873022
- Applicant / Sponsor: J R Scientific
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.2220
- Decision date: 1987-08-19
Classification & Regulation
This clearance is catalogued under FDA product code KIT and 21 CFR 864.2220, within the Hematology review panel as a Class I device.