510(k) K810311

STERI-VERS by The Hilrad Co. — Product Code LDS

K810311 is an FDA 510(k) premarket notification submitted by The Hilrad Co. for the device "STERI-VERS". The FDA issued a decision of Substantially Equivalent on April 17, 1981. The device falls under product code LDS (Device, Pasteurization, Hot Water), a Class II device regulated under 21 CFR 880.6991.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 17, 1981
Date Received
February 5, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Pasteurization, Hot Water
Device Class
Class II
Regulation Number
880.6991
Review Panel
HO
Submission Type