510(k) K904694

CUSTOMED ANGIODRAPE PACK FEMORAL by Customed, Inc. — Product Code KKX

K904694 is an FDA 510(k) premarket notification submitted by Customed, Inc. for the device "CUSTOMED ANGIODRAPE PACK FEMORAL". The FDA issued a decision of Substantially Equivalent (kit) on January 2, 1991. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. Customed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESK (Substantially Equivalent (kit))
Decision Date
January 2, 1991
Date Received
October 16, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drape, Surgical, Antimicrobial
Device Class
Class II
Regulation Number
878.4370
Review Panel
HO
Submission Type

Surgical drapes with an antimicrobial agent are subject to 510(k) review, under the procedures established by the 21st Century Cures Act. This product code is the class II non-exempt counterpart of PUI.