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FDA 510(k)

DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)

K-Number: K031329 · 2003-10-22

ApplicantDynatronics Corp.
Decision Date2003-10-22
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY) is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 2003-10-22 under 510(k) number K031329. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)?

DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY) is a medical device that received FDA 510(k) clearance on 2003-10-22. The listed applicant is Dynatronics Corp.. The 510(k) number is K031329.

When did DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY) receive FDA 510(k) clearance?

DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY) received FDA 510(k) clearance on 2003-10-22, under 510(k) number K031329.

Who is the listed applicant for DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)?

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 SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)?

The FDA product code for DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY) is IMI.

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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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