510(k) K093553

Device: POSTURETEK
Applicant: PERSEUS ALTHETICS,LLC
510(k) number: K093553
Product code: LZW
Decision: Substantially Equivalent (SESE)
Decision date: 2010-08-13
Date received: 2009-11-17
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: Summary
Third party reviewed: No

Related Records

Applicant Contact

Contact: KEITH BARRITT
Address: 1425 K St., NW, Suite 1100 Washington DC US 20005 20005

Source Documents

Other 510(k) Records For Product Code LZW

510(k)	Device	Applicant	Decision date
K081540	ZEGRA POSTURE TRAINER	Peter Fischer	2009-02-20
K951244	SPINE TUNER POSTURE TRAINER	Dan Kline	1995-06-26
K902669	BPA, BODY POSITION ALARM	Bagrad	1990-07-27
K884976	MICRO-STRAIGHT POSTURE TRAINING DEVICE	Mcdowell Ent., Inc.	1989-06-09

Legacy Summary

summary

FDA Review

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