510(k) K160451

V. A.C. VeraFlo Cleanse Choice Dressing System for use with the V.A.C. Ulta ... by Kci USA, Inc. (Kinetic Concepts, Inc.) — Product Code OMP

K160451 is an FDA 510(k) premarket notification submitted by Kci USA, Inc. (Kinetic Concepts, Inc.) for the device "V. A.C. VeraFlo Cleanse Choice Dressing System for use with the V.A.C. Ulta ...". The FDA issued a decision of Substantially Equivalent on Jun 20, 2016. The device falls under product code OMP (Negative Pressure Wound Therapy Powered Suction Pump), a Class II device regulated under 21 CFR 878.4780. Kci USA, Inc. (Kinetic Concepts, Inc.) has 12 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Jun 20, 2016
Date Received
Feb 18, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Negative Pressure Wound Therapy Powered Suction Pump
Device Class
Class II
Regulation Number
878.4780
Review Panel
SU
Submission Type
510(k)

For wound management via application of continual or intermittent negative pressure to the wound for removal of fluids, including wound exudate, irrigation fluids, and infectious materials. The Device is indicated for management of chronic, acute, traumatic, subacute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts.