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FDA 510(k)

DYNATRON 2000

K-Number: K880912 · 1988-03-15

ApplicantDynatronics Corp.
Decision Date1988-03-15
Product CodeIKE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNATRON 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 1988-03-15 under 510(k) number K880912. The device is classified under product code IKE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRON 2000?

DYNATRON 2000 is a medical device that received FDA 510(k) clearance on 1988-03-15. The listed applicant is Dynatronics Corp.. The 510(k) number is K880912.

When did DYNATRON 2000 receive FDA 510(k) clearance?

DYNATRON 2000 received FDA 510(k) clearance on 1988-03-15, under 510(k) number K880912.

Who is the listed applicant for DYNATRON 2000?

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 2000?

The FDA product code for DYNATRON 2000 is IKE.

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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: IKE)

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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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