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510(k) K902669

Device
BPA, BODY POSITION ALARM
Applicant
BAGRAD
510(k) number
K902669
Product code
LZW  
Decision
Substantially Equivalent (SESE)
Decision date
1990-07-27
Date received
1990-06-18
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
Third party reviewed
No

Related Records

Applicant Contact

Contact
SHAWN GALLAGHER
Address
375 Glendening Rd. Orange Park FL US 32073 32073

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
K951244SPINE TUNER POSTURE TRAINERDan Kline1995-06-26
K884976MICRO-STRAIGHT POSTURE TRAINING DEVICEMcdowell Ent., Inc.1989-06-09

Legacy Summary

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FDA Review

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