The following data is part of a premarket notification filed by Math Resolutions, Llc. with the FDA for Dosimetry Check.
Device ID | K010225 |
510k Number | K010225 |
Device Name: | DOSIMETRY 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 | 2001-01-24 |
Decision Date | 2001-04-24 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
B229DC051 | K010225 | 000 |
B229DC041 | K010225 | 000 |