SERIES-5 MyoVision Full System D2-D5-D6-D7L

GUDID 00853818007422

VisionHub with FlexVision Inclinometers, DynaVision Dynamic sEMG and ScanVision Static sEMG Scanner

PRECISION BIOMETRICS INC

Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier Multiple physiological signal amplifier
Primary Device ID00853818007422
NIH Device Record Key852fe694-b496-4b7d-9a70-28660f4b4548
Commercial Distribution StatusIn Commercial Distribution
Brand NameSERIES-5 MyoVision Full System
Version Model NumberD2-D5-D6-D7L
Catalog NumberD2-D5-D6-D7L
Company DUNS362997926
Company NamePRECISION BIOMETRICS INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com
Phone800-969-6961
Emailadmin@myovision.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100853818007422 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KQXGoniometer, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-03-08
Device Publish Date2021-02-28

Devices Manufactured by PRECISION BIOMETRICS INC

00853818007477 - MyoVision Software2022-11-18 Software
00853818007460 - MyoVision Wirefree System2021-05-25 VisionHUB with DynaVision Dynamic sEMG
00853818007422 - SERIES-5 MyoVision Full System2021-03-08VisionHub with FlexVision Inclinometers, DynaVision Dynamic sEMG and ScanVision Static sEMG Scanner
00853818007422 - SERIES-5 MyoVision Full System2021-03-08 VisionHub with FlexVision Inclinometers, DynaVision Dynamic sEMG and ScanVision Static sEMG Scanner
00853818007439 - SERIES-5 MyoVision ScanVision2021-03-08 SERIES-5 VisionHUB with ScanVision Static sEMG Scanner
00853818007446 - SERIES-5 MyoVision ScanVision2021-03-08 SERIES-5 VisionHUB with ScanVision Static sEMG Scanners
00853818007453 - SERIES-5 MyoVision FlexVision System2021-03-08 SERIES-5 VisionHUB with FlexVision Inclinometers
00853818007415 - MyoVision Wirefree System2021-01-13 VisionHub with FlexVision Inclinometers and DynaVision Dynamic sEMG
00853818007330 - USB Charger2020-02-06 USB Wall Charger

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.