meddevicedb.com FDA Device Reference

SPECIALTY ASSAYED CONTROL-1

K941737 Class II Traditional
Decision Date
1994-10-07
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K941737
Product Code GIZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5425
Decision Date 1994-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECIALTY ASSAYED CONTROL-1 received FDA 510(k) clearance under submission number K941737, sponsored by Helena Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1994-10-07.

Classification & Regulation

This clearance is catalogued under FDA product code GIZ and 21 CFR 864.5425, within the Hematology review panel as a Class II device.