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FDA 510(k)

ELECTROPULSE - LOW BACK PAIN

K-Number: K062532 · 2007-02-09

Decision Date2007-02-09
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROPULSE - LOW BACK PAIN is the device name listed in this FDA 510(k) record. The listed applicant is Pain Relief Technologies. It received FDA 510(k) clearance on 2007-02-09 under 510(k) number K062532. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROPULSE - LOW BACK PAIN?

ELECTROPULSE - LOW BACK PAIN is a medical device that received FDA 510(k) clearance on 2007-02-09. The listed applicant is Pain Relief Technologies. The 510(k) number is K062532.

When did ELECTROPULSE - LOW BACK PAIN receive FDA 510(k) clearance?

ELECTROPULSE - LOW BACK PAIN received FDA 510(k) clearance on 2007-02-09, under 510(k) number K062532.

Who is the listed applicant for ELECTROPULSE - LOW BACK PAIN?

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

What is the FDA product code for ELECTROPULSE - LOW BACK PAIN?

The FDA product code for ELECTROPULSE - LOW BACK PAIN is NUH.

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.

Other records listing Pain Relief Technologies as applicant

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.

Related Devices (Code: NUH)

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.

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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