510(k) K821525

DESERET UNIVERSAL LUER LOCK by Warner-Lambert Co. — Product Code KGZ

K821525 is an FDA 510(k) premarket notification submitted by Warner-Lambert Co. for the device "DESERET UNIVERSAL LUER LOCK". The FDA issued a decision of Substantially Equivalent on June 23, 1982. The device falls under product code KGZ (Accessories, Catheter), a Class I device regulated under 21 CFR 878.4200. Warner-Lambert Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 23, 1982
Date Received
May 21, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, Catheter
Device Class
Class I
Regulation Number
878.4200
Review Panel
SU
Submission Type