meddevicedb.com FDA Device Reference

CPK (UV) REAGENT KIT

K855188 Class II Traditional
Decision Date
1986-03-05
Sponsor / Applicant
Technostics Intl.

Technical Specification

510(k) Submission ID K855188
Product Code JHS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1986-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CPK (UV) REAGENT KIT received FDA 510(k) clearance under submission number K855188, sponsored by Technostics Intl.. 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 1986-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code JHS and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.