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 |