K925956 is an FDA 510(k) clearance for the MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT. This device is classified as a System, Applicator, Radionuclide, Remote-controlled (Class II - Special Controls, product code JAQ).
Submitted by Nucletron-Oldelft Corp. (Columbia, US). The FDA issued a Cleared decision on November 19, 1993, 360 days after receiving the submission on November 24, 1992.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.5700.
| 510(k) Number | K925956 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 24, 1992 |
| Decision Date | November 19, 1993 |
| Days to Decision | 360 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Statement |
| Product Code | JAQ — System, Applicator, Radionuclide, Remote-controlled |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.5700 |