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FDA 510(k)

Smith & Nephew 25 Fluid Management System

K-Number: K171794 · 2017-06-27

Decision Date2017-06-27
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Smith & Nephew 25 Fluid Management System is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2017-06-27 under 510(k) number K171794. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Smith & Nephew 25 Fluid Management System?

Smith & Nephew 25 Fluid Management System is a medical device that received FDA 510(k) clearance on 2017-06-27. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K171794.

When did Smith & Nephew 25 Fluid Management System receive FDA 510(k) clearance?

Smith & Nephew 25 Fluid Management System received FDA 510(k) clearance on 2017-06-27, under 510(k) number K171794.

Who is the listed applicant for Smith & Nephew 25 Fluid Management System?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Smith & Nephew 25 Fluid Management System?

The FDA product code for Smith & Nephew 25 Fluid Management System is HRX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Smith & Nephew, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: HRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.