VERDICT PCP— 510(k) K963692
Substantially EquivalentEditek, Inc.
FDA 510(k) clearance K963692 for VERDICT PCP, Substantially Equivalent on 1996-12-10. Applicant: Editek, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Editek, Inc.
- Product code
- Code LCM
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Burlington, NC, US
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