FOOT SWITCH

GUDID 08809502330033

VIOL Co.,Ltd.

Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system

Primary Device ID	08809502330033
NIH Device Record Key	cd22418a-c48c-4dae-b842-c3974dfbf61b
Commercial Distribution Status	In Commercial Distribution
Brand Name	FOOT SWITCH
Version Model Number	F/S
Company DUNS	695654949
Company Name	VIOL Co.,Ltd.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	true
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809502330033 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K172023

FDA Product Code

GEI	Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2021-01-15
Device Publish Date	2018-04-02

On-Brand Devices [FOOT SWITCH]

08809502330033	F/S
08809502330187	F/S-B