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 |