LIQUICORD— 510(k) K092384
Substantially EquivalentCentrix, Inc.
FDA 510(k) clearance K092384 for LIQUICORD, Substantially Equivalent on 2009-11-04. 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
Recent devices under product code MVL
view allMore clearances from Centrix, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.