meddevicedb.com FDA Device Reference

NEONATAL NTSH RADIOIMMUNOASSAY SYS

K830036 Class II Traditional
Decision Date
1983-01-28
Sponsor / Applicant
Corning Medical & Scientific

Technical Specification

510(k) Submission ID K830036
Product Code JLW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1690
Decision Date 1983-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEONATAL NTSH RADIOIMMUNOASSAY SYS received FDA 510(k) clearance under submission number K830036, sponsored by Corning Medical & Scientific. 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 1983-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code JLW and 21 CFR 862.1690, within the Clinical Chemistry review panel as a Class II device.