510(k) K082297

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

K082297 is an FDA 510(k) premarket notification submitted by Busse Hospital Disposables, Inc. for the device "BUSSE SURGICAL DRAPE". The FDA issued a decision of Substantially Equivalent on December 9, 2008. 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
December 9, 2008
Date Received
August 12, 2008
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.