meddevicedb.com FDA Device Reference

CHROM Z-HEPARIN, CAT. NO 5242

K952667 Class II Traditional
Decision Date
1996-02-14
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K952667
Product Code KFF
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7525
Decision Date 1996-02-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHROM Z-HEPARIN, CAT. NO 5242 received FDA 510(k) clearance under submission number K952667, 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 1996-02-14.

Classification & Regulation

This clearance is catalogued under FDA product code KFF and 21 CFR 864.7525, within the Hematology review panel as a Class II device.