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 |