Alcopro Inc

FDA Filings

This page includes the latest FDA filings for Alcopro Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number1054127
FEI Number1000112835
NameAlcoPro Inc
Owner & OperatorAlcoPro Inc
Contact Address2547 Sutherland Ave
Knoxville TN 37919 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2547 Sutherland Ave
Knoxville, TN 37919 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Alcopro Inc.
Checkpoint CCP084102022-09-30
Alcopro Inc.
Checkpoint CCP082002022-09-30
Alcopro Inc.
Checkpoint CCP044102022-09-30
Alcopro Inc.
Checkpoint CCP042002022-09-30
Alcopro Inc.
Checkpoint CCP024102022-09-30
Alcopro Inc.
Checkpoint CCP022002022-09-30
Alcopro Inc.
AlcoBreath Tube AAB15402022-09-30
Alcopro Inc.
AlcoBreath Tube AAB15202022-09-30
Alcopro Inc.
AlcoBreath Tube AAB08402022-09-30
Alcopro Inc.
AlcoBreath Tube AAB08202022-09-30
AlcoPro Inc
SAFEWAY2011-06-21
AlcoPro Inc
CheckPoint2011-06-21
AlcoPro Inc
BreathIQ2011-06-21
AlcoPro Inc
AlcoCheck2011-06-21
AlcoPro Inc
Alco-Breath Tube2011-06-21
ALCOPRO, INC.
ALCO-BREATH TUBE, CHECKPOINT BREATH ALCOHOL TEST2011-04-06

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