MULTIPLE

Accelerator, Linear, Medical

LARSON MEDICAL PRODUCTS, INC.

The following data is part of a premarket notification filed by Larson Medical Products, Inc. with the FDA for Multiple.

Pre-market Notification Details

Device IDK112460
510k NumberK112460
Device Name:MULTIPLE
ClassificationAccelerator, Linear, Medical
Applicant LARSON MEDICAL PRODUCTS, INC. 80 WESTGATE DRIVE Newark,  OH  43055
ContactPeter Larson
CorrespondentPeter Larson
LARSON MEDICAL PRODUCTS, INC. 80 WESTGATE DRIVE Newark,  OH  43055
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2011-08-26
Decision Date2011-10-07

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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Trademark Results [MULTIPLE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MULTIPLE
MULTIPLE
98361511 not registered Live/Pending
FBA Private Market, LLC
2024-01-17
MULTIPLE
MULTIPLE
98017886 not registered Live/Pending
PRL Inc.
2023-05-29
MULTIPLE
MULTIPLE
85965618 4881951 Live/Registered
Multiple, Inc.
2013-06-20
MULTIPLE
MULTIPLE
85347383 4418998 Live/Registered
Universal Cooperatives, Inc.
2011-06-15
MULTIPLE
MULTIPLE
85317632 not registered Dead/Abandoned
LING-LING PAN
2011-05-11
MULTIPLE
MULTIPLE
75300895 2369683 Dead/Cancelled
Iwata Denko Co., Ltd.
1997-05-30

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