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510(k) K951244

Device
SPINE TUNER POSTURE TRAINER
Applicant
DAN KLINE
510(k) number
K951244
Product code
LZW  
Decision
Substantially Equivalent (SESE)
Decision date
1995-06-26
Date received
1995-03-13
Regulation
510(k) Premarket Notification
Classification name
Monitor, Spine Curvature
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
Physical Medicine
Device class
U
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
DAN KLINE
Address
1816 W. Cliff Ct. Carlsbad CA US 92008 92008

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LZW  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K093553POSTURETEKPerseus Althetics,Llc2010-08-13
K081540ZEGRA POSTURE TRAINERPeter Fischer2009-02-20
K902669BPA, BODY POSITION ALARMBagrad1990-07-27
K884976MICRO-STRAIGHT POSTURE TRAINING DEVICEMcdowell Ent., Inc.1989-06-09

Legacy Summary#

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FDA Review#

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