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FDA 510(k)

ELECTROPULSE-COSMETIC

K-Number: K113724 · 2012-02-15

ApplicantPain Relief Technologies
Decision Date2012-02-15
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROPULSE-COSMETIC 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 2012-02-15 under 510(k) number K113724. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROPULSE-COSMETIC?

ELECTROPULSE-COSMETIC is a medical device that received FDA 510(k) clearance on 2012-02-15. The listed applicant is Pain Relief Technologies. The 510(k) number is K113724.

When did ELECTROPULSE-COSMETIC receive FDA 510(k) clearance?

ELECTROPULSE-COSMETIC received FDA 510(k) clearance on 2012-02-15, under 510(k) number K113724.

Who is the listed applicant for ELECTROPULSE-COSMETIC?

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-COSMETIC?

The FDA product code for ELECTROPULSE-COSMETIC is NFO.

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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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.

K062532ELECTROPULSE - LOW BACK PAINK051128ELECTROPULSE

Related Devices (Code: NFO)

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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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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