The following data is part of a premarket notification filed by Larson Medical Products, Inc. with the FDA for Multiple.
| Device ID | K112460 |
| 510k Number | K112460 |
| Device Name: | MULTIPLE |
| Classification | Accelerator, Linear, Medical |
| Applicant | LARSON MEDICAL PRODUCTS, INC. 80 WESTGATE DRIVE Newark, OH 43055 |
| Contact | Peter Larson |
| Correspondent | Peter Larson LARSON MEDICAL PRODUCTS, INC. 80 WESTGATE DRIVE Newark, OH 43055 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-08-26 |
| Decision Date | 2011-10-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MULTIPLE 98361511 not registered Live/Pending |
FBA Private Market, LLC 2024-01-17 |
![]() MULTIPLE 98017886 not registered Live/Pending |
PRL Inc. 2023-05-29 |
![]() MULTIPLE 85965618 4881951 Live/Registered |
Multiple, Inc. 2013-06-20 |
![]() MULTIPLE 85347383 4418998 Live/Registered |
Universal Cooperatives, Inc. 2011-06-15 |
![]() MULTIPLE 85317632 not registered Dead/Abandoned |
LING-LING PAN 2011-05-11 |
![]() MULTIPLE 75300895 2369683 Dead/Cancelled |
Iwata Denko Co., Ltd. 1997-05-30 |