meddevicedb.com FDA Device Reference

EZ DETECH-URINE BLOOD TEST STICKS

K854358 Class II Traditional
Decision Date
1986-04-09
Sponsor / Applicant
Self Care Systems, Inc.

Technical Specification

510(k) Submission ID K854358
Product Code KHE
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6550
Decision Date 1986-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EZ DETECH-URINE BLOOD TEST STICKS received FDA 510(k) clearance under submission number K854358, sponsored by Self Care Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1986-04-09.

Classification & Regulation

This clearance is catalogued under FDA product code KHE and 21 CFR 864.6550, within the Hematology review panel as a Class II device.