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FDA 510(k)

RENASYS DYNAFLOW Kit (66807741)

K-Number: K261338 · 2026-09-11

Decision Date2026-09-11
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RENASYS DYNAFLOW Kit (66807741) is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Medical, Ltd.. It received FDA 510(k) clearance on 2026-09-11 under 510(k) number K261338. 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 RENASYS DYNAFLOW Kit (66807741)?

RENASYS DYNAFLOW Kit (66807741) is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Smith & Nephew Medical, Ltd.. The 510(k) number is K261338.

When did RENASYS DYNAFLOW Kit (66807741) receive FDA 510(k) clearance?

RENASYS DYNAFLOW Kit (66807741) received FDA 510(k) clearance on 2026-09-11, under 510(k) number K261338.

Who is the listed applicant for RENASYS DYNAFLOW Kit (66807741)?

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

What is the FDA product code for RENASYS DYNAFLOW Kit (66807741)?

The FDA product code for RENASYS DYNAFLOW Kit (66807741) is OMP.

Other records listing Smith & Nephew Medical, Ltd. 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.

View all 29 devices →

Related Devices (Code: OMP)

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

View on FDA Database →

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