Medline Reusable Blood Pressure Cuff
K-Number: K254287 · 2026-06-22
Device Summary
Frequently Asked Questions
What is the Medline Reusable Blood Pressure Cuff?
Medline Reusable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2026-06-22. The listed applicant is Medline Industries, LP. The 510(k) number is K254287.
When did Medline Reusable Blood Pressure Cuff receive FDA 510(k) clearance?
Medline Reusable Blood Pressure Cuff received FDA 510(k) clearance on 2026-06-22, under 510(k) number K254287.
Who is the listed applicant for Medline Reusable Blood Pressure Cuff?
The FDA 510(k) record lists Medline Industries, LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medline Reusable Blood Pressure Cuff?
The FDA product code for Medline Reusable Blood Pressure Cuff is DXQ.
Other records listing Medline Industries, LP 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.
Related Devices (Code: DXQ)
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.