MINIBLASTER

Airbrush

DELDENT LTD.

The following data is part of a premarket notification filed by Deldent Ltd. with the FDA for Miniblaster.

Pre-market Notification Details

Device IDK013969
510k NumberK013969
Device Name:MINIBLASTER
ClassificationAirbrush
Applicant DELDENT LTD. 19 KEREN KAYEMET ST. Petach Tikvah,  IL 49372
ContactAlan Edel
CorrespondentAlan Edel
DELDENT LTD. 19 KEREN KAYEMET ST. Petach Tikvah,  IL 49372
Product CodeKOJ  
CFR Regulation Number872.6080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2001-12-03
Decision Date2002-01-10

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
10840326418502 K013969 000
10816577020368 K013969 000
10816577020375 K013969 000
10816577020382 K013969 000
10840326403515 K013969 000
10840326418458 K013969 000
10840326418465 K013969 000
10840326418472 K013969 000
10840326418489 K013969 000
10840326418496 K013969 000
10816577020344 K013969 000

Trademark Results [MINIBLASTER]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MINIBLASTER
MINIBLASTER
78751754 not registered Dead/Abandoned
JLab Audio, Inc.
2005-11-10
MINIBLASTER
MINIBLASTER
77433859 3523966 Live/Registered
Artistry In Motion, Inc.
2008-03-27

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