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FDA 510(k)

DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE

K-Number: K051261 · 2005-07-25

ApplicantDynatronics Corp.
Decision Date2005-07-25
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 2005-07-25 under 510(k) number K051261. 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 DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE?

DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE is a medical device that received FDA 510(k) clearance on 2005-07-25. The listed applicant is Dynatronics Corp.. The 510(k) number is K051261.

When did DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE receive FDA 510(k) clearance?

DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE received FDA 510(k) clearance on 2005-07-25, under 510(k) number K051261.

Who is the listed applicant for DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE?

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

What is the FDA product code for DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE?

The FDA product code for DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE is ILY.

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Other records listing Dynatronics Corp. 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.

K113250DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEK060814DYNATRON ION IONTOPHORESIS ELECTRODEK051680DYNATRON DX2 TRACTION UNITK043047DYNATRON IBOX IONTOPHORESIS DEVICEK040729SOLARIS D890 THERAPY PROBEK031329DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)

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Related Devices (Code: ILY)

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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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