CORDCAP— 510(k) K091380
Substantially EquivalentCentrix, Inc.
FDA 510(k) clearance K091380 for CORDCAP, Substantially Equivalent on 2009-07-30. Applicant: Centrix, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Centrix, Inc.
- Product code
- Code MVL
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, US
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