The following data is part of a premarket notification filed by Medimage, Inc. with the FDA for M-link.
Device ID | K922303 |
510k Number | K922303 |
Device Name: | M-LINK |
Classification | System, Tomography, Computed, Emission |
Applicant | MEDIMAGE, INC. 6276 JACKSON RD. STE. G Ann Arbor, MI 48103 -9579 |
Contact | William C Forgacs |
Correspondent | William C Forgacs MEDIMAGE, INC. 6276 JACKSON RD. STE. G Ann Arbor, MI 48103 -9579 |
Product Code | KPS |
CFR Regulation Number | 892.1200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-15 |
Decision Date | 1992-12-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
M-LINK 87590217 not registered Live/Pending |
FW MURPHY PRODUCTION CONTROLS, LLC 2017-08-30 |
M-LINK 78392958 not registered Dead/Abandoned |
ATI Technologies Inc. 2004-03-30 |
M-LINK 78337132 not registered Dead/Abandoned |
9150-5115 QUEBEC INC. 2003-12-05 |
M-LINK 77725165 3897777 Dead/Cancelled |
Medtronic, Inc. 2009-04-29 |
M-LINK 75657406 2675323 Dead/Cancelled |
INTELLI-CHECK, INC. 1999-10-05 |
M-LINK 74516450 not registered Dead/Abandoned |
Multi Service Corporation 1994-04-25 |