JVC

GUDID 00046838002694

CL-S600BA0UA

JVC KENWOOD CORPORATION

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Primary Device ID00046838002694
NIH Device Record Key566e33db-3038-4b6c-867b-1381ca839c6e
Commercial Distribution StatusIn Commercial Distribution
Brand NameJVC
Version Model NumberCL-S600
Company DUNS713321040
Company NameJVC KENWOOD CORPORATION
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 Datetrue
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
GS100046838002694 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PGYDisplay, Diagnostic Radiology

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-01-10
Device Publish Date2022-01-01

On-Brand Devices [JVC]

00046838081033MS-S500
00046838081026CL-S500
00046838081941MS-S300
00046838002212MS-S200BN0UA
00046838002205MS-S200BF0UA
00046838002120CL-S1200BGUA
00046838002694CL-S600BA0UA
00046838079979MS-S500
00046838079962CL-S500
00046838078897CL-R211
00046838078880CL-S200
00046838077531CL-S300
00046838077524CL-S300
00046838076626CCL214
00046838076619CCL650i2/AR
00046838076602CCL650i2/N
00046838076596CCL258i2/F
00046838076589CCL258i2/AR
00046838076572CCL258i2/N
00046838076565MS25i2/AR
00046838076558MS25i2/N
00046838076541MS25i2/F
00046838076534MS35i2/AR
00046838076527MS35i2/N
00046838076510MS35i2/F
00046838076435MS55i2 plus
00046838076411MS55i2 plus
00046838076381CCL550i2/F
00046838076374CCL550i2/N
00046838076367CCL358i2/F
00046838076350CCL358i2/N
00046838002687CL-R813BN0UA

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