meddevicedb.com FDA Device Reference

BLOOD GROUPING SYS., BG-9

K771098 Class II Traditional
Decision Date
1977-08-04
Sponsor / Applicant
Technicon Instruments Corp.

Technical Specification

510(k) Submission ID K771098
Product Code KSZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.9175
Decision Date 1977-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD GROUPING SYS., BG-9 received FDA 510(k) clearance under submission number K771098, sponsored by Technicon Instruments Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1977-08-04.

Classification & Regulation

This clearance is catalogued under FDA product code KSZ and 21 CFR 864.9175, within the Hematology review panel as a Class II device.