FDA 510(k)

Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)

Numéro K : K251745 · 2025-12-16

Date de décision2025-12-16

Code produitDXQ

Comité consultatifCV

DécisionSubstantially Equivalent

Résumé du dispositif

Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2025-12-16 under 510(k) number K251745. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)?

Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) is a medical device that received FDA 510(k) clearance on 2025-12-16. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K251745.

When did Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) receive FDA 510(k) clearance?

Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) received FDA 510(k) clearance on 2025-12-16, under 510(k) number K251745.

Who is the listed applicant for Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)?

The FDA 510(k) record lists Baxter Healthcare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)?

The FDA product code for Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) is DXQ.

Essais cliniques associés

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Dispositifs connexes (Code : DXQ)

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Source officielle

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