The following data is part of a premarket notification filed by Larson Products, Inc. with the FDA for Klarity.
Device ID | K022708 |
510k Number | K022708 |
Device Name: | KLARITY |
Classification | Accelerator, Linear, Medical |
Applicant | LARSON PRODUCTS, INC. 2844 BANWICK RD. Columbus, OH 43232 -2115 |
Contact | Peter M Larson |
Correspondent | Peter M Larson LARSON PRODUCTS, INC. 2844 BANWICK RD. Columbus, OH 43232 -2115 |
Product Code | IYE |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-08-14 |
Decision Date | 2002-11-12 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
KLARITY 98577818 not registered Live/Pending |
Klarity Intelligence, Inc. 2024-05-31 |
KLARITY 90371989 not registered Live/Pending |
Demand Science Group, LLC 2020-12-10 |
KLARITY 90371966 not registered Live/Pending |
Demand Science Group, LLC 2020-12-10 |
KLARITY 88454898 not registered Live/Pending |
C.R. Laurence Co., Inc. 2019-05-31 |
KLARITY 77873211 3852624 Live/Registered |
KLARITY MEDICAL PRODUCTS, LLC 2009-11-16 |
KLARITY 77702869 not registered Dead/Abandoned |
Lindstrom, Richard L. 2009-03-31 |
KLARITY 76151674 not registered Dead/Abandoned |
KrystalBox Technologies, Inc 2000-10-23 |
KLARITY 76151621 not registered Dead/Abandoned |
KrystalBox Technologies, Inc. 2000-10-23 |
KLARITY 75488515 2366912 Live/Registered |
KLA-Tencor Corporation 1998-05-18 |
KLARITY 75393512 2217283 Dead/Cancelled |
LARSON PRODUCTS, INC. 1997-11-20 |