DEKA TAC DEVICE— 510(k) K093915
Substantially EquivalentDeka Research & Development Corp.
FDA 510(k) clearance K093915 for DEKA TAC DEVICE, Substantially Equivalent on 2011-08-23. Applicant: Deka Research & Development Corp.. Device class: 2.
Clearance details
- Applicant
- Deka Research & Development Corp.
- Product code
- Code FIG
- Device class
- Class 2
- Regulation
- 21 CFR 876.5820
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Manchester, NH, US
Recent devices under product code FIG
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