PICO Single Use Negative Pressure Wound Therapy System
K-Number: K172519 · 2017-09-15
ApplicantSmith & Nephew Medical Limited
Decision Date2017-09-15
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
PICO Single Use Negative Pressure Wound Therapy System is a medical device manufactured by Smith & Nephew Medical Limited. It received FDA 510(k) clearance on 2017-09-15 under approval number K172519. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PICO Single Use Negative Pressure Wound Therapy System?
PICO Single Use Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2017-09-15. It is manufactured by Smith & Nephew Medical Limited. The 510(k) number is K172519.
When was PICO Single Use Negative Pressure Wound Therapy System approved by the FDA?
PICO Single Use Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2017-09-15, under approval number K172519.
What company makes PICO Single Use Negative Pressure Wound Therapy System?
PICO Single Use Negative Pressure Wound Therapy System is manufactured by Smith & Nephew Medical Limited.
What is the FDA product code for PICO Single Use Negative Pressure Wound Therapy System?
The FDA product code for PICO Single Use Negative Pressure Wound Therapy System is OMP.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.