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FDA 510(k)

DYNATRON STS RX

K-Number: K010948 · 2001-05-15

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

Device Summary

DYNATRON STS RX 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 K010948. 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 RX?

DYNATRON STS RX 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 K010948.

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

DYNATRON STS RX received FDA 510(k) clearance on 2001-05-15, under 510(k) number K010948.

Who is the listed applicant for DYNATRON STS RX?

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 RX?

The FDA product code for DYNATRON STS RX 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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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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