Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Welch Allyn Connex Central Station

K-Number: K212473 · 2022-10-28

ApplicantWelch Allyn, Inc.
Decision Date2022-10-28
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Welch Allyn Connex Central Station is a medical device manufactured by Welch Allyn, Inc.. It received FDA 510(k) clearance on 2022-10-28 under approval number K212473. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Welch Allyn Connex Central Station?

Welch Allyn Connex Central Station is a medical device that received FDA 510(k) clearance on 2022-10-28. It is manufactured by Welch Allyn, Inc.. The 510(k) number is K212473.

When was Welch Allyn Connex Central Station approved by the FDA?

Welch Allyn Connex Central Station received FDA 510(k) clearance on 2022-10-28, under approval number K212473.

What company makes Welch Allyn Connex Central Station?

Welch Allyn Connex Central Station is manufactured by Welch Allyn, Inc..

What is the FDA product code for Welch Allyn Connex Central Station?

The FDA product code for Welch Allyn Connex Central Station is MWI.

Related Clinical Trials

NCT07501611 Acute Cardiovascular Effects of Transcutaneous Auricular Vagus Nerve Stimulation NOT_YET_RECRUITING

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 K223381iExaminer System with Panoptic Plus K241411Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM) K243598Welch Allyn Connex® 360 (Multiple)

View all 7 devices →

Related Devices (Code: MWI)

K161909IQvitals ZoneMidmark Corporation K160718Vital Sync Informatics Manager & Virtual Patient Monitoring PlatformCovidien K151839AMC Health VitalCaregiving SystemAmc Health K160956LD-Oxi systemLd Technology, LLC K153739MRI Patient Monitor TeslaDUOMipm Mammendorfer Institut Fur Physik Und Medizin K153225Masimo Root Monitoring System and AccessoriesMasimo Corporation

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.

↑