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FDA 510(k)

POSTURETEK

K-Number: K093553 · 2010-08-13

ApplicantPerseus Althetics,Llc
Decision Date2010-08-13
Product CodeLZW
DecisionSubstantially Equivalent

Device Summary

POSTURETEK is the device name listed in this FDA 510(k) record. The listed applicant is Perseus Althetics,Llc. It received FDA 510(k) clearance on 2010-08-13 under 510(k) number K093553. The device is classified under product code LZW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSTURETEK?

POSTURETEK is a medical device that received FDA 510(k) clearance on 2010-08-13. The listed applicant is Perseus Althetics,Llc. The 510(k) number is K093553.

When did POSTURETEK receive FDA 510(k) clearance?

POSTURETEK received FDA 510(k) clearance on 2010-08-13, under 510(k) number K093553.

Who is the listed applicant for POSTURETEK?

The FDA 510(k) record lists Perseus Althetics,Llc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSTURETEK?

The FDA product code for POSTURETEK is LZW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: LZW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K081540ZEGRA POSTURE TRAINERPeter FischerK951244SPINE TUNER POSTURE TRAINERDan KlineK902669BPA, BODY POSITION ALARMBagradK884976MICRO-STRAIGHT POSTURE TRAINING DEVICEMcdowell Ent., Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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