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FDA 510(k)

BPA, BODY POSITION ALARM

K-Number: K902669 · 1990-07-27

ApplicantBagrad
Decision Date1990-07-27
Product CodeLZW
DecisionSubstantially Equivalent

Device Summary

BPA, BODY POSITION ALARM is the device name listed in this FDA 510(k) record. The listed applicant is Bagrad. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K902669. The device is classified under product code LZW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BPA, BODY POSITION ALARM?

BPA, BODY POSITION ALARM is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Bagrad. The 510(k) number is K902669.

When did BPA, BODY POSITION ALARM receive FDA 510(k) clearance?

BPA, BODY POSITION ALARM received FDA 510(k) clearance on 1990-07-27, under 510(k) number K902669.

Who is the listed applicant for BPA, BODY POSITION ALARM?

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

What is the FDA product code for BPA, BODY POSITION ALARM?

The FDA product code for BPA, BODY POSITION ALARM is LZW.

Related Clinical Trials

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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 FischerK951244SPINE TUNER POSTURE TRAINERDan KlineK884976MICRO-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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