The following data is part of a premarket notification filed by Cnmc Company Incorporated with the FDA for Model 206 Electrometer/dosimeter.
Device ID | K150265 |
510k Number | K150265 |
Device Name: | Model 206 Electrometer/Dosimeter |
Classification | Accelerator, Linear, Medical |
Applicant | CNMC COMPANY INCORPORATED 865 EASTHAGEN DRIVE Nashville, TN 37217 |
Contact | Thomas Kraus |
Correspondent | Thomas Kraus CNMC COMPANY INCORPORATED 865 EASTHAGEN DRIVE Nashville, TN 37217 |
Product Code | IYE |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-02-04 |
Decision Date | 2015-09-03 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00862246000301 | K150265 | 000 |
08622460003012 | K150265 | 000 |