GENESIS REUSABLE RIGID CONTAINER SYSTEM— 510(k) K140850
Substantially EquivalentCarefusion 2200, Inc.
FDA 510(k) clearance K140850 for GENESIS REUSABLE RIGID CONTAINER SYSTEM, Substantially Equivalent on 2014-08-27. Applicant: Carefusion 2200, Inc.. Device class: 2.
Clearance details
- Applicant
- Carefusion 2200, Inc.
- Product code
- Code KCT
- Device class
- Class 2
- Regulation
- 21 CFR 880.6850
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vernon Hills, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.