Welch Allyn Connex® 360 (Multiple)
Summary
Welch Allyn, Inc. received 510(k) clearance for Welch Allyn Connex® 360 (Multiple), a device. Cleared on 2025-07-13.
Details
Source
510(k) Clearance
External ID
K243598
Action Date
2025-07-13
Status
Traditional
Category
device
Product Description
Welch Allyn Connex® 360 (Multiple). Product code: .
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Welch Allyn, Inc. has received 4 total clearances in our database.
Welch Allyn, Inc. has 5 FDA actions in our database, including 1 recall and 4 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Welch Allyn, Inc. have FDA actions?
Welch Allyn, Inc. has 5 FDA actions in our database, including 1 recall and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K243598" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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