meddevicedb.com FDA Device Reference

BETA/PAK

K790769 Class II Traditional
Decision Date
1979-05-03
Sponsor / Applicant
Bio/Data Corp.

Technical Specification

510(k) Submission ID K790769
Product Code JOZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5700
Decision Date 1979-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BETA/PAK received FDA 510(k) clearance under submission number K790769, sponsored by Bio/Data 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 1979-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code JOZ and 21 CFR 864.5700, within the Hematology review panel as a Class II device.