DEKA TAC DEVICE— 510(k) K093915

Substantially Equivalent

Deka Research & Development Corp.

FDA 510(k) clearance K093915 for DEKA TAC DEVICE, Substantially Equivalent on 2011-08-23. Applicant: Deka Research & Development Corp..

Clearance details

Applicant: Deka Research & Development Corp.
Product code: Code FIG
Advisory panel: Gastroenterology, Urology
Date received: 2009-12-22
Decision date: 2011-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Manchester, NH, US

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