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FDA 510(k)

THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE

K-Number: K070024 · 2007-05-16

ApplicantThor International
Decision Date2007-05-16
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Thor International. It received FDA 510(k) clearance on 2007-05-16 under 510(k) number K070024. 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 THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE?

THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE is a medical device that received FDA 510(k) clearance on 2007-05-16. The listed applicant is Thor International. The 510(k) number is K070024.

When did THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE receive FDA 510(k) clearance?

THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE received FDA 510(k) clearance on 2007-05-16, under 510(k) number K070024.

Who is the listed applicant for THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE?

The FDA 510(k) record lists Thor International as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE?

The FDA product code for THOR VR SINGLE DIODE LASER TREATMENT PROBE, MODEL 200 MW SINGLE VR DIODE PROBE is ILY.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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