VeriQuick

GUDID 00049696609531

FOURSTAR GROUP INC.

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Primary Device ID00049696609531
NIH Device Record Keyee0b7e2f-c9cb-426f-a855-5684150ab2cf
Commercial Distribution StatusIn Commercial Distribution
Brand NameVeriQuick
Version Model Number171444
Company DUNS656091279
Company NameFOURSTAR GROUP INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does n
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100049696609531 [Primary]

FDA Product Code

LCXKit, Test, Pregnancy, Hcg, Over The Counter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-19

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00049696609531171444
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00004969673664At Home Marijuana Test Kit
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0004969673784511012637
0004969673783811012450S
0004969673773911012450MB
00049696128032PREGNANCY TEST 2CT
00049696739344MULTI-DRUG URINE TEST DIP CARD
00049696708319AT HOME MULTI-DRUG TEST

Trademark Results [VeriQuick]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERIQUICK
VERIQUICK
86639057 4877560 Live/Registered
Fourstar Group Inc.
2015-05-22

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