510(k) K060200

MICROTEK MEDICAL WARMING DRAPE by Microtek Medical, Inc. — Product Code KKX

K060200 is an FDA 510(k) premarket notification submitted by Microtek Medical, Inc. for the device "MICROTEK MEDICAL WARMING DRAPE". The FDA issued a decision of Substantially Equivalent on May 31, 2006. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. Microtek Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 31, 2006
Date Received
January 26, 2006
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.