510(k) K940175

MEDSURG STERILE O.R. TOWELS by Medsurg Industries, Inc. — Product Code KKX

K940175 is an FDA 510(k) premarket notification submitted by Medsurg Industries, Inc. for the device "MEDSURG STERILE O.R. TOWELS". The FDA issued a decision of Substantially Equivalent on May 26, 1994. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. Medsurg Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 26, 1994
Date Received
January 11, 1994
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.