The following data is part of a premarket notification filed by Math Resolutions, Llc. with the FDA for Dusimetry Check.
| Device ID | K101503 |
| 510k Number | K101503 |
| Device Name: | DUSIMETRY CHECK |
| Classification | Accelerator, Linear, Medical |
| Applicant | MATH RESOLUTIONS, LLC. 5975 GALES LN. Columbia, MD 21045 |
| Contact | Wendel D Renner |
| Correspondent | Wendel D Renner MATH RESOLUTIONS, LLC. 5975 GALES LN. Columbia, MD 21045 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-06-01 |
| Decision Date | 2010-08-04 |
| Summary: | summary |