510(k) K092212

BUSSE SURGICAL DRAPES III by Busse Hospital Disposables, Inc. — Product Code KKX

K092212 is an FDA 510(k) premarket notification submitted by Busse Hospital Disposables, Inc. for the device "BUSSE SURGICAL DRAPES III". The FDA issued a decision of Substantially Equivalent on October 9, 2009. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. Busse Hospital Disposables, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 9, 2009
Date Received
July 22, 2009
Clearance Type
Special
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.