VERDICT PCP— 510(k) K963692

Substantially Equivalent

Editek, 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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