The following data is part of a premarket notification filed by Hamilton Thorne Research with the FDA for Fotomaster.
Device ID | K000380 |
510k Number | K000380 |
Device Name: | FOTOMASTER |
Classification | System, Image Processing, Radiological |
Applicant | HAMILTON THORNE RESEARCH 100 CUMMINGS CENTER SUITE 102-C Beverly, MA 01915 |
Contact | Meg D Hamilton |
Correspondent | Meg D Hamilton HAMILTON THORNE RESEARCH 100 CUMMINGS CENTER SUITE 102-C Beverly, MA 01915 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-02-07 |
Decision Date | 2000-05-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FOTOMASTER 85654959 not registered Dead/Abandoned |
Fotomoto, Inc. 2012-06-18 |