meddevicedb.com FDA Device Reference

TEST CELLS

K790249 Class II Traditional
Decision Date
1979-05-16
Sponsor / Applicant
Hyland Therapeutic Div., Travenol Laboratories

Technical Specification

510(k) Submission ID K790249
Product Code KSF
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.9650
Decision Date 1979-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEST CELLS received FDA 510(k) clearance under submission number K790249, sponsored by Hyland Therapeutic Div., Travenol 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 1979-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code KSF and 21 CFR 864.9650, within the Hematology review panel as a Class II device.