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FDA 510(k)

SPINE TUNER POSTURE TRAINER

K-Number: K951244 · 1995-06-26

ApplicantDan Kline
Decision Date1995-06-26
Product CodeLZW
DecisionSubstantially Equivalent

Device Summary

SPINE TUNER POSTURE TRAINER is the device name listed in this FDA 510(k) record. The listed applicant is Dan Kline. It received FDA 510(k) clearance on 1995-06-26 under 510(k) number K951244. The device is classified under product code LZW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINE TUNER POSTURE TRAINER?

SPINE TUNER POSTURE TRAINER is a medical device that received FDA 510(k) clearance on 1995-06-26. The listed applicant is Dan Kline. The 510(k) number is K951244.

When did SPINE TUNER POSTURE TRAINER receive FDA 510(k) clearance?

SPINE TUNER POSTURE TRAINER received FDA 510(k) clearance on 1995-06-26, under 510(k) number K951244.

Who is the listed applicant for SPINE TUNER POSTURE TRAINER?

The FDA 510(k) record lists Dan Kline as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPINE TUNER POSTURE TRAINER?

The FDA product code for SPINE TUNER POSTURE TRAINER is LZW.

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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.

K093553POSTURETEKPerseus Althetics,LlcK081540ZEGRA POSTURE TRAINERPeter FischerK902669BPA, BODY POSITION ALARMBagradK884976MICRO-STRAIGHT POSTURE TRAINING DEVICEMcdowell Ent., Inc.

Official Source

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

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