EPLEY OMNIAX— 510(k) K071973
Substantially EquivalentVesticon
FDA 510(k) clearance K071973 for EPLEY OMNIAX, Substantially Equivalent on 2008-06-20. Applicant: Vesticon. Device class: Unclassified.
Clearance details
- Applicant
- Vesticon
- Product code
- Code LXV
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Portland, OR, US
Recent devices under product code LXV
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