FDA.report

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

Related Records

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)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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