meddevicedb.com FDA Device Reference

BIOPHEN PROTEIN C5, C2.5, MODELS 221205, 221202

K050365 Class II Traditional
Decision Date
2005-12-27
Sponsor / Applicant
Hyphen Biomed

Technical Specification

510(k) Submission ID K050365
Product Code GGP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7290
Decision Date 2005-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOPHEN PROTEIN C5, C2.5, MODELS 221205, 221202 received FDA 510(k) clearance under submission number K050365, sponsored by Hyphen Biomed. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2005-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code GGP and 21 CFR 864.7290, within the Hematology review panel as a Class II device.