meddevicedb.com FDA Device Reference

MRI HCG-BETA RIA KIT CAT. #MR-10100

K801491 Class II Traditional
Decision Date
1980-08-13
Sponsor / Applicant
Microanalytic Research, Inc.

Technical Specification

510(k) Submission ID K801491
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1980-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MRI HCG-BETA RIA KIT CAT. #MR-10100 received FDA 510(k) clearance under submission number K801491, sponsored by Microanalytic Research, 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 1980-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code JHI and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.