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FDA 510(k)

Welch Allyn Connex® 360 (Multiple)

K-Number: K243598 · 2025-07-13

ApplicantWelch Allyn, Inc.
Decision Date2025-07-13
Product Code
DecisionSubstantially Equivalent

Device Summary

Welch Allyn Connex® 360 (Multiple) is a medical device manufactured by Welch Allyn, Inc.. It received FDA 510(k) clearance on 2025-07-13 under approval number K243598. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Welch Allyn Connex® 360 (Multiple)?

Welch Allyn Connex® 360 (Multiple) is a medical device that received FDA 510(k) clearance on 2025-07-13. It is manufactured by Welch Allyn, Inc.. The 510(k) number is K243598.

When was Welch Allyn Connex® 360 (Multiple) approved by the FDA?

Welch Allyn Connex® 360 (Multiple) received FDA 510(k) clearance on 2025-07-13, under approval number K243598.

What company makes Welch Allyn Connex® 360 (Multiple)?

Welch Allyn Connex® 360 (Multiple) is manufactured by Welch Allyn, Inc..

Other Devices by Welch Allyn, Inc.

K171621Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System, 901060 Vital Signs Monitor K181016Welch Allyn RetinaVue Network REF 901108 PACS Medical Image System K191013Welch Allyn Diagnostic Cardiology Suite 2.X.X with Spirometry option K212473Welch Allyn Connex Central Station K223381iExaminer System with Panoptic Plus K241411Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)

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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.

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