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FDA 510(k)

Pain Therapy System, Model PTS-II

K-Number: K150277 · 2016-02-12

Decision Date2016-02-12
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Pain Therapy System, Model PTS-II is the device name listed in this FDA 510(k) record. The listed applicant is Counter Scientific Development (Gz), Ltd.. It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K150277. 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 Pain Therapy System, Model PTS-II?

Pain Therapy System, Model PTS-II is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Counter Scientific Development (Gz), Ltd.. The 510(k) number is K150277.

When did Pain Therapy System, Model PTS-II receive FDA 510(k) clearance?

Pain Therapy System, Model PTS-II received FDA 510(k) clearance on 2016-02-12, under 510(k) number K150277.

Who is the listed applicant for Pain Therapy System, Model PTS-II?

The FDA 510(k) record lists Counter Scientific Development (Gz), Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pain Therapy System, Model PTS-II?

The FDA product code for Pain Therapy System, Model PTS-II is NUH.

Other records listing Counter Scientific Development (Gz), Ltd. 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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