Prospera Spectruum Negative Pressure Wound Therapy System

FDA 510(k) K230233 · Deroyal Industries, Inc.

Substantially Equivalent

510(k) numberK230233

Submission

Device name
Prospera Spectruum Negative Pressure Wound Therapy System
Applicant
Deroyal Industries, Inc.
Powell, TN, US
Received
January 27, 2023
Decision date
April 18, 2024
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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K253429Genadyne ASTRA NPWTOMP · Traditional Genadyne Biotechnologies, Inc.03/12/2026SE
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K251646extriCARE® 1000 Negative Pressure Wound Therapy SystemOMP · Traditional Alleva Medical Devices10/03/2025SE
K251826RENASYS WOUND+ Dressing Kit with AIRLOCK TechnologyOMP · Traditional Smith & Nephew Medical, Ltd.09/11/2025SE

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K191425Hydro-Temp Neonatal Skin Temperature Probe CoverFMT · Traditional 01/21/2020SE
K173072Algidex Ag Silver Alginate Wound DressingFRO · Traditional 04/04/2018SE
K171475DeRoyal Laprador Specimen Retrieval SystemGCJ · Traditional 08/17/2017SE
K152978DeRoyal Angiography KitsDXT · Traditional 03/25/2016SESK
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Questions and answers

When was Prospera Spectruum Negative Pressure Wound Therapy System cleared by the FDA?

Prospera Spectruum Negative Pressure Wound Therapy System (K230233) received a 510(k) decision of Substantially Equivalent on April 18, 2024, 447 days after the submission was received.

What is the product code of K230233?

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.