HEMATOXYLIN II

Hematoxylin

VOLU SOL MEDICAL INDUSTRIES

The following data is part of a premarket notification filed by Volu Sol Medical Industries with the FDA for Hematoxylin Ii.

Pre-market Notification Details

Device IDK821540
510k NumberK821540
Device Name:HEMATOXYLIN II
ClassificationHematoxylin
Applicant VOLU SOL MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeHYJ  
CFR Regulation Number864.1850 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-05-24
Decision Date1982-06-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.