The following data is part of a premarket notification filed by Canon Medical Systems Corporation with the FDA for Mr Elastography; Mzek-001a.
Device ID | K220018 |
510k Number | K220018 |
Device Name: | MR Elastography; MZEK-001A |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | Canon Medical Systems Corporation 1385 Shimoishigami Otawara-shi, JP 324-8550 |
Contact | Paul Biggins |
Correspondent | Paul Biggins Canon Medical Systems USA 2441 Michelle Drive Tustin, CA 92780 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-01-05 |
Decision Date | 2022-03-03 |