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PROTEIN C REAGENT

K002541 Class II Traditional
Decision Date
2000-09-26
Sponsor / Applicant
Dade Behring, Inc.

Technical Specification

510(k) Submission ID K002541
Product Code GGP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7290
Decision Date 2000-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROTEIN C REAGENT received FDA 510(k) clearance under submission number K002541, sponsored by Dade Behring, 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 2000-09-26.

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.