510(k) K932277

LONZA FORMULATION R-82 by Calgon Vestal Div. — Product Code LRJ

K932277 is an FDA 510(k) premarket notification submitted by Calgon Vestal Div. for the device "LONZA FORMULATION R-82". The FDA issued a decision of Substantially Equivalent on May 12, 1994. The device falls under product code LRJ (Disinfectant, Medical Devices), a Class I device regulated under 21 CFR 880.6890. Calgon Vestal Div. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 12, 1994
Date Received
May 12, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Disinfectant, Medical Devices
Device Class
Class I
Regulation Number
880.6890
Review Panel
HO
Submission Type