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FDA 510(k)

MU PHOTONICS PAIN THERAPIST

K-Number: K012508 · 2001-10-09

ApplicantNu Photonics, Inc.
Decision Date2001-10-09
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MU PHOTONICS PAIN THERAPIST is the device name listed in this FDA 510(k) record. The listed applicant is Nu Photonics, Inc.. It received FDA 510(k) clearance on 2001-10-09 under 510(k) number K012508. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MU PHOTONICS PAIN THERAPIST?

MU PHOTONICS PAIN THERAPIST is a medical device that received FDA 510(k) clearance on 2001-10-09. The listed applicant is Nu Photonics, Inc.. The 510(k) number is K012508.

When did MU PHOTONICS PAIN THERAPIST receive FDA 510(k) clearance?

MU PHOTONICS PAIN THERAPIST received FDA 510(k) clearance on 2001-10-09, under 510(k) number K012508.

Who is the listed applicant for MU PHOTONICS PAIN THERAPIST?

The FDA 510(k) record lists Nu Photonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MU PHOTONICS PAIN THERAPIST?

The FDA product code for MU PHOTONICS PAIN THERAPIST is ILY.

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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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