Karman Healthcare

GUDID 00810058400017

XO-202 16" Full Power Stand Up Chair

KARMAN HEALTHCARE INC.

Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible
Primary Device ID00810058400017
NIH Device Record Keya67edd94-89cf-4123-91e2-fd9d7d6afd55
Commercial Distribution StatusIn Commercial Distribution
Brand NameKarman Healthcare
Version Model NumberXO-202N
Company DUNS878092667
Company NameKARMAN HEALTHCARE INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810058400017 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ITIWheelchair, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-18
Device Publish Date2020-08-10

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