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FDA 510(k)

SOLARIS D890 THERAPY PROBE

K-Number: K040729 · 2004-06-02

ApplicantDynatronics Corp.
Decision Date2004-06-02
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SOLARIS D890 THERAPY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 2004-06-02 under 510(k) number K040729. 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 SOLARIS D890 THERAPY PROBE?

SOLARIS D890 THERAPY PROBE is a medical device that received FDA 510(k) clearance on 2004-06-02. The listed applicant is Dynatronics Corp.. The 510(k) number is K040729.

When did SOLARIS D890 THERAPY PROBE receive FDA 510(k) clearance?

SOLARIS D890 THERAPY PROBE received FDA 510(k) clearance on 2004-06-02, under 510(k) number K040729.

Who is the listed applicant for SOLARIS D890 THERAPY PROBE?

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 SOLARIS D890 THERAPY PROBE?

The FDA product code for SOLARIS D890 THERAPY PROBE 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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