Prytime Medical Devices Inc

FDA Filings

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

FDA Registration(s)
Registration Number3012279212
FEI Number3012279212
NamePRYTIME MEDICAL DEVICES, INC.
Owner & OperatorPrytime Medical Devices, Inc.
Contact Address229 North Main Street
Boerne TX 78006 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address13949 W Colfax Ave Ste 110
Lakewood, CO 80401 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
Prytime Medical Devices, Inc.
PREBOA-PRO Catheter2020-06-03
Prytime Medical Devices, Inc
ER-REBOA PLUS Catheter2020-01-09
PRYTIME MEDICAL DEVICES, INC.
ER-REBOA Catheter ER7232A2019-03-21
PRYTIME MEDICAL DEVICES, INC.
Access Kit with 5 Fr Mini Access Set2019-01-24
PRYTIME MEDICAL DEVICES, INC.
Access Kit with 18 Ga Arterial Catheterization Set2019-01-24
Prytime Medical Devices, Inc.
ER-REBOA Catheter2017-11-08
PRYTIME MEDICAL DEVICES, INC.
ER-REBOA Catheter Convenience Set with Pressure Monitoring2017-05-03
PRYTIME MEDICAL DEVICES, INC.
ER-REBOA Catheter Convenience Kit2017-05-03
Prytime Medical Devices, Inc
ER-REBOA Catheter2017-04-04
PRYTIME MEDICAL DEVICES, INC.
ER-REBOA Catheter2015-12-27
PRYTIME MEDICAL DEVICES, INC.
ER-REBOA Catheter2015-12-27

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