Pulsenmore ES— 510(k) DEN240074
UnknownPulsenmore, Ltd.
FDA 510(k) clearance DEN240074 for Pulsenmore ES, Unknown on 2025-10-31. Applicant: Pulsenmore, Ltd.. Device class: 2.
Clearance details
- Applicant
- Pulsenmore, Ltd.
- Product code
- Code SGJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1590
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Omer, IL
Data sourced from openFDA. This site is unofficial and independent of the FDA.