meddevicedb.com FDA Device Reference

CELL-CHEX

K780140 Class II Traditional
Decision Date
1978-03-27
Sponsor / Applicant
Streck Laboratories, Inc.

Technical Specification

510(k) Submission ID K780140
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 1978-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CELL-CHEX received FDA 510(k) clearance under submission number K780140, sponsored by Streck Laboratories, 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 1978-03-27.

Classification & Regulation

This clearance is catalogued under FDA product code JPK and 21 CFR 864.8625, within the Hematology review panel as a Class II device.