Access BR Monitor— 510(k) K240403
Substantially EquivalentBeckman Coulter, Inc.
FDA 510(k) clearance K240403 for Access BR Monitor, Substantially Equivalent on 2024-05-09. Applicant: Beckman Coulter, Inc.. Device class: 2.
Clearance details
- Applicant
- Beckman Coulter, Inc.
- Product code
- Code MOI
- Device class
- Class 2
- Regulation
- 21 CFR 866.6010
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chaska, MN, US
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