Clearance Summary
DYNATECH MR 300 MANUAL MICROELISA received FDA 510(k) clearance under submission number K874244, sponsored by Dynatech Laboratories, 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 1987-11-03.
- Submission: K874244
- Applicant / Sponsor: Dynatech Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2300
- Decision date: 1987-11-03
Classification & Regulation
This clearance is catalogued under FDA product code JJQ and 21 CFR 862.2300, within the Clinical Chemistry review panel as a Class I device.