meddevicedb.com FDA Device Reference

FACTOR X DEFICIENT PLASMA, BLOD HUMAN

K843310 Class II Traditional
Decision Date
1984-11-19
Sponsor / Applicant
Sigma Chemical Co.

Technical Specification

510(k) Submission ID K843310
Product Code GGP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7290
Decision Date 1984-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FACTOR X DEFICIENT PLASMA, BLOD HUMAN received FDA 510(k) clearance under submission number K843310, sponsored by Sigma Chemical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1984-11-19.

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.