Venturi Gauze Wound Care Sets with Portal Drain

FDA 510(k) K151263 · Talley Group, Ltd.

Substantially Equivalent

510(k) numberK151263

Submission

Device name
Venturi Gauze Wound Care Sets with Portal Drain
Applicant
Talley Group, Ltd.
Romsey, GB
Received
May 13, 2015
Decision date
February 19, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OMP – Negative Pressure Wound Therapy Powered Suction Pump
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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.

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K914774Multipulse Sequential Compression UnitIRP · Traditional 02/11/1992SE
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K914776Oxford Pressure Monitor/Talley Pressure MonitorJFC · Traditional 12/19/1991SE

Questions and answers

When was Venturi Gauze Wound Care Sets with Portal Drain cleared by the FDA?

Venturi Gauze Wound Care Sets with Portal Drain (K151263) received a 510(k) decision of Substantially Equivalent on February 19, 2016, 282 days after the submission was received.

What is the product code of K151263?

The FDA product code is OMP – Negative Pressure Wound Therapy Powered Suction Pump, a Class II (moderate risk) device regulated under 21 CFR 878.4780.