Medline Reusable Blood Pressure Cuff— 510(k) K254287

Name: FDA 510(k) clearance K254287
Creator: U.S. Food and Drug Administration
Published: 2026-06-22

Substantially Equivalent

Medline Industries, LP

FDA 510(k) clearance K254287 for Medline Reusable Blood Pressure Cuff, Substantially Equivalent on 2026-06-22. Applicant: Medline Industries, LP. Device class: 2.

Summary

The Medline Reusable Blood Pressure Cuff from Medline Industries is filed under DXQ, blood pressure cuffs. The record gives no sizes or model numbers.

Class II, 21 CFR 870.1120. Cardiovascular is both the classification panel and the review panel. It was a Traditional 510(k).

Medline filed from Northfiled, Illinois, as the record spells the city. Review took 173 calendar days (December 31, 2025 to June 22, 2026).

Clearance details

Applicant: Medline Industries, LP
Product code: Product code DXQ
Device class: Class 2
Regulation: 21 CFR 870.1120
Advisory panel: Cardiovascular
Date received: 2025-12-31
Decision date: 2026-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northfiled, IL, US

Medline Reusable Blood Pressure Cuff— 510(k) K254287

Summary

Clearance details

Recent devices under product code DXQ

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