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FDA 510(k)

DYNATRON STS

K-Number: K010565 · 2001-05-15

ApplicantDynatronics Corp.
Decision Date2001-05-15
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DYNATRON STS is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 2001-05-15 under 510(k) number K010565. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRON STS?

DYNATRON STS is a medical device that received FDA 510(k) clearance on 2001-05-15. The listed applicant is Dynatronics Corp.. The 510(k) number is K010565.

When did DYNATRON STS receive FDA 510(k) clearance?

DYNATRON STS received FDA 510(k) clearance on 2001-05-15, under 510(k) number K010565.

Who is the listed applicant for DYNATRON STS?

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 STS?

The FDA product code for DYNATRON STS is LIH.

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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.

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Related Devices (Code: LIH)

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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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