510(k) K820542

SURGIKOS INCISE DRAPE by Surgikos, Inc. — Product Code KKX

K820542 is an FDA 510(k) premarket notification submitted by Surgikos, Inc. for the device "SURGIKOS INCISE DRAPE". The FDA issued a decision of Substantially Equivalent on June 2, 1982. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. Surgikos, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 2, 1982
Date Received
March 2, 1982
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.