510(k) K031131

KLINIDRAPE SURGICAL DRAPES by Molnlycke Health Care — Product Code KKX

K031131 is an FDA 510(k) premarket notification submitted by Molnlycke Health Care for the device "KLINIDRAPE SURGICAL DRAPES". The FDA issued a decision of Substantially Equivalent on June 10, 2003. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. Molnlycke Health Care has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 10, 2003
Date Received
April 9, 2003
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.