K243598
- 510(k) number
- K243598
- Device name
- Welch Allyn Connex® 360 (Multiple)
- Applicant
- Welch Allyn, Inc. NY · US
- Decision date
- 2025-07-13
- Date received
- 2024-11-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
510(k) Summary (official FDA PDF): K243598.pdf
Official FDA record: K243598
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.