510(k) K934630

UNIVERSAL VIDEO/LASER ARM DRAPE by Hydro-Med Products, Inc. — Product Code KKX

K934630 is an FDA 510(k) premarket notification submitted by Hydro-Med Products, Inc. for the device "UNIVERSAL VIDEO/LASER ARM DRAPE". The FDA issued a decision of Substantially Equivalent on October 28, 1994. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. Hydro-Med Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 28, 1994
Date Received
September 24, 1993
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.