VISI-PITCH

GUDID 04961333245390

v4.0 VISI-PITCH WIN10 UPGRADE

PENTAX OF AMERICA, INC.

Electroglottograph
Primary Device ID04961333245390
NIH Device Record Key18c93b05-a503-4661-8a4e-21ecec123e56
Commercial Distribution StatusIn Commercial Distribution
Brand NameVISI-PITCH
Version Model Number3950WU
Company DUNS083211284
Company NamePENTAX OF AMERICA, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104961333245390 [Primary]

FDA Product Code

KLXElectroglottograph

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-08-06
Device Publish Date2018-07-05

On-Brand Devices [VISI-PITCH]

04961333245390v4.0 VISI-PITCH WIN10 UPGRADE
04961333244621VISI-PITCH IV (JAPAN)
04961333236572VISI-PITCH (SOFTWARE)
04961333235438VISI-PITCH

Trademark Results [VISI-PITCH]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VISI-PITCH
VISI-PITCH
73204908 1135661 Dead/Cancelled
KAY ELEMETRICS CORP.
1979-02-23

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