The following data is part of a premarket notification filed by Unipath Ltd. with the FDA for Clearplan.
Device ID | K871332 |
510k Number | K871332 |
Device Name: | CLEARPLAN |
Classification | Radioimmunoassay, Luteinizing Hormone |
Applicant | UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
Contact | George Zajicek |
Correspondent | George Zajicek UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
Product Code | CEP |
CFR Regulation Number | 862.1485 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-04-03 |
Decision Date | 1987-08-05 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CLEARPLAN 90229172 not registered Live/Pending |
ClearPlan LLC 2020-10-01 |
CLEARPLAN 86468730 4781334 Live/Registered |
CLEARPLAN LLC 2014-12-02 |
CLEARPLAN 78903409 not registered Dead/Abandoned |
Tom, Raymond 2006-06-08 |
CLEARPLAN 77424371 4078434 Dead/Cancelled |
USA Tax & Insurance Services, Inc. 2008-03-17 |
CLEARPLAN 77399056 3902456 Dead/Cancelled |
Tom, Raymond 2008-02-16 |
CLEARPLAN 73617772 1496356 Dead/Cancelled |
UNIPATH LIMITED 1986-09-02 |