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FDA 510(k)

DYNATRON DX2 TRACTION UNIT

K-Number: K051680 · 2005-10-11

ApplicantDynatronics Corp.
Decision Date2005-10-11
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNATRON DX2 TRACTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 2005-10-11 under 510(k) number K051680. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRON DX2 TRACTION UNIT?

DYNATRON DX2 TRACTION UNIT is a medical device that received FDA 510(k) clearance on 2005-10-11. The listed applicant is Dynatronics Corp.. The 510(k) number is K051680.

When did DYNATRON DX2 TRACTION UNIT receive FDA 510(k) clearance?

DYNATRON DX2 TRACTION UNIT received FDA 510(k) clearance on 2005-10-11, under 510(k) number K051680.

Who is the listed applicant for DYNATRON DX2 TRACTION UNIT?

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 DX2 TRACTION UNIT?

The FDA product code for DYNATRON DX2 TRACTION UNIT is ILY.

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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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