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FDA 510(k)

MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1

K-Number: K032928 · 2003-12-19

ApplicantMediphysics Pain Centers of America
Decision Date2003-12-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1 is the device name listed in this FDA 510(k) record. The listed applicant is Mediphysics Pain Centers of America. It received FDA 510(k) clearance on 2003-12-19 under 510(k) number K032928. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1?

MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1 is a medical device that received FDA 510(k) clearance on 2003-12-19. The listed applicant is Mediphysics Pain Centers of America. The 510(k) number is K032928.

When did MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1 receive FDA 510(k) clearance?

MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1 received FDA 510(k) clearance on 2003-12-19, under 510(k) number K032928.

Who is the listed applicant for MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1?

The FDA 510(k) record lists Mediphysics Pain Centers of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1?

The FDA product code for MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1 is GZJ.

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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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