510(k) K821533

HEMATOXYLIN I by Volu Sol Medical Industries — Product Code HYJ

K821533 is an FDA 510(k) premarket notification submitted by Volu Sol Medical Industries for the device "HEMATOXYLIN I". The FDA issued a decision of Substantially Equivalent on June 10, 1982. The device falls under product code HYJ (Hematoxylin), a Class I device regulated under 21 CFR 864.1850. Volu Sol Medical Industries has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 10, 1982
Date Received
May 21, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hematoxylin
Device Class
Class I
Regulation Number
864.1850
Review Panel
PA
Submission Type