meddevicedb.com FDA Device Reference

VOLU-SOL STATIM STAIN

K792497 Class I Traditional
Decision Date
1979-12-18
Sponsor / Applicant
Volu Sol Medical Industries

Technical Specification

510(k) Submission ID K792497
Product Code IAF
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.1850
Decision Date 1979-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VOLU-SOL STATIM STAIN received FDA 510(k) clearance under submission number K792497, sponsored by Volu Sol Medical Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1979-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code IAF and 21 CFR 864.1850, within the Hematology review panel as a Class I device.