The following data is part of a premarket notification filed by Diamond Diagnostics, Inc. with the FDA for Mission Complete.
| Device ID | K060206 |
| 510k Number | K060206 |
| Device Name: | MISSION COMPLETE |
| Classification | Multi-analyte Controls, All Kinds (assayed) |
| Applicant | DIAMOND DIAGNOSTICS, INC. 333 FISKE ST. Holliston, MA 01746 |
| Contact | Randolph Quinn |
| Correspondent | Randolph Quinn DIAMOND DIAGNOSTICS, INC. 333 FISKE ST. Holliston, MA 01746 |
| Product Code | JJY |
| CFR Regulation Number | 862.1660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-01-26 |
| Decision Date | 2006-03-21 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MISSION COMPLETE 76213266 not registered Dead/Abandoned |
ECHO TOYS LTD. 2001-02-22 |