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 |