The following data is part of a premarket notification filed by Diamond Diagnostics, Inc. with the FDA for Mission Controls.
Device ID | K033063 |
510k Number | K033063 |
Device Name: | MISSION CONTROLS |
Classification | Controls For Blood-gases, (assayed And Unassayed) |
Applicant | DIAMOND DIAGNOSTICS, INC. 331 FISKE ST. Holliston, MA 01746 |
Contact | Linda M Stundtner |
Correspondent | Linda M Stundtner DIAMOND DIAGNOSTICS, INC. 331 FISKE ST. Holliston, MA 01746 |
Product Code | JJS |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-09-29 |
Decision Date | 2003-12-12 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MISSION CONTROLS 75787463 2447510 Dead/Cancelled |
Mission Controls Automation, Inc. 1999-08-30 |
MISSION CONTROLS 75787442 2433084 Dead/Cancelled |
Mission Controls Automation, Inc. 1999-08-30 |