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510(k) K960843

Device
STOP-N-GROW
Applicant
EUROPEAN TOUCH CO., INC.
510(k) number
K960843
Product code
MQZ  
Decision
Substantially Equivalent (SESE)
Decision date
1996-08-12
Date received
1996-02-29
Regulation
510(k) Premarket Notification
Classification name
Prosthesis, Nail
Medical specialty
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Review panel
General & Plastic Surgery
Device class
U
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
MATT WALKER
Address
5203 N. 125th St. Butler WI US 53007 53007

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code MQZ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K230841NailLiftJps Corporation2024-01-22
K162525Oniko nail braceBegum Saglik Hizmetleri Tibbi Malzemeler Danismanlik Lsti2018-04-25
K850803NAIL SPLINTInro Medical Designs, Inc.1985-10-16

Legacy Summary#

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FDA Review#

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