ELECTROPULSE - LOW BACK PAIN
K-Number: K062532 · 2007-02-09
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Device Summary
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
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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