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FDA 510(k)

DYNATRON 950

K-Number: K950349 · 1995-09-13

ApplicantDynatronics Corp.
Decision Date1995-09-13
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent for Some Indications

Device Summary

DYNATRON 950 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 1995-09-13 under 510(k) number K950349. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DYNATRON 950?

DYNATRON 950 is a medical device that received FDA 510(k) clearance on 1995-09-13. The listed applicant is Dynatronics Corp.. The 510(k) number is K950349.

When did DYNATRON 950 receive FDA 510(k) clearance?

DYNATRON 950 received FDA 510(k) clearance on 1995-09-13, under 510(k) number K950349.

Who is the listed applicant for DYNATRON 950?

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 950?

The FDA product code for DYNATRON 950 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.

K113250DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEK060814DYNATRON ION IONTOPHORESIS ELECTRODEK051680DYNATRON DX2 TRACTION UNITK051261DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBEK043047DYNATRON IBOX IONTOPHORESIS DEVICEK040729SOLARIS D890 THERAPY PROBE

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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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