Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System, 901060 Vital Signs Monitor— 510(k) K171621

Substantially Equivalent

Welch Allyn, Inc.

FDA 510(k) clearance K171621 for Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System, 901060 Vital Signs Monitor, Substantially Equivalent on 2017-06-30. Applicant: Welch Allyn, Inc.. Device class: 2.

Clearance details

Applicant
Welch Allyn, Inc.
Product code
Code MHX
Device class
Class 2
Regulation
21 CFR 870.1025
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Skaneateles Falls, NY, US
Download summary PDFView on FDA.gov ↗

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More clearances from Welch Allyn, Inc.

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Adverse events under product code MHX

product code MHX
Death
580
Injury
2,441
Malfunction
12,655
Other
3
Total
15,679

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K171621

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K171621.

Data sourced from openFDA. This site is unofficial and independent of the FDA.