510(k) K132741

V.A.C. VIA NEGATIVE PRESSURE WOUND THERAPY SYSTEM by Kci USA, Inc. — Product Code OMP

K132741 is an FDA 510(k) premarket notification submitted by Kci USA, Inc. for the device "V.A.C. VIA NEGATIVE PRESSURE WOUND THERAPY SYSTEM". The FDA issued a decision of Substantially Equivalent on November 15, 2013. 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. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 15, 2013
Date Received
September 3, 2013
Clearance Type
Special
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

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.