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ELVI 810 CLOTSCANNER

K791587 Class II Traditional
Decision Date
1979-09-17
Sponsor / Applicant
Volu Sol Medical Industries

Technical Specification

510(k) Submission ID K791587
Product Code KQG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5400
Decision Date 1979-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELVI 810 CLOTSCANNER received FDA 510(k) clearance under submission number K791587, 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 1979-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code KQG and 21 CFR 864.5400, within the Hematology review panel as a Class II device.