The following data is part of a premarket notification filed by Medical Graphics Corp. with the FDA for Express Series.
Device ID | K070858 |
510k Number | K070858 |
Device Name: | EXPRESS SERIES |
Classification | Computer, Oxygen-uptake |
Applicant | MEDICAL GRAPHICS CORP. 350 OAK GROVE PKWY. St. Paul, MN 55127 -8599 |
Contact | Mary E Donlin |
Correspondent | Mary E Donlin MEDICAL GRAPHICS CORP. 350 OAK GROVE PKWY. St. Paul, MN 55127 -8599 |
Product Code | BZL |
CFR Regulation Number | 868.1730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-03-28 |
Decision Date | 2007-04-16 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
B3687000239060 | K070858 | 000 |
B368700023905 | K070858 | 000 |
00810016250005 | K070858 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EXPRESS SERIES 98693921 not registered Live/Pending |
D.R. Horton, Inc. 2024-08-12 |
EXPRESS SERIES 97877893 not registered Live/Pending |
Woodtone Industries USA 2023-04-07 |
EXPRESS SERIES 75478905 2646034 Dead/Cancelled |
3M COMPANY 1998-05-04 |
EXPRESS SERIES 75297689 not registered Dead/Abandoned |
Menasha Corporation 1997-05-23 |
EXPRESS SERIES 74230553 1798547 Dead/Cancelled |
PANAVISE PRODUCTS, INC. 1991-12-16 |