Welch Allyn Connex® 360 (Multiple)
FDA 510(k) clearance K243598 · decided 2025-07-13
Clearance details
- K-number
- K243598
- Device name
- Welch Allyn Connex® 360 (Multiple)
- Applicant
- Welch Allyn, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2024-11-21
- Decision date
- 2025-07-13
- Days to decision
- 234 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Skaneateles Falls, NY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.