K090135 is an FDA 510(k) clearance for the TRIMIRA IDENTAFI 3000. This device is classified as a Diagnostic Light, Soft Tissue Detector (Class II - Special Controls, product code NXV).
Submitted by Remicalm, LLC (Houston, US). The FDA issued a Cleared decision on February 17, 2009, 27 days after receiving the submission on January 21, 2009.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6350. To Be Used As An Aid In The Detection Or Visualization Of Abnormalities Of Intraoral Soft Tissue. An Adjunct To Traditional Intraoral Examination By Incandescent Light To Enhance The Visualization Of Oral Mucosal Abnormalities.
| 510(k) Number | K090135 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 21, 2009 |
| Decision Date | February 17, 2009 |
| Days to Decision | 27 days |
| Submission Type | Special |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | NXV — Diagnostic Light, Soft Tissue Detector |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.6350 |
| Definition | To Be Used As An Aid In The Detection Or Visualization Of Abnormalities Of Intraoral Soft Tissue. An Adjunct To Traditional Intraoral Examination By Incandescent Light To Enhance The Visualization Of Oral Mucosal Abnormalities |