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FDA 510(k)

TH0R DDII IR LAMP SYSTEM

K-Number: K033923 · 2004-03-17

ApplicantThor Intl.
Decision Date2004-03-17
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TH0R DDII IR LAMP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Thor Intl.. It received FDA 510(k) clearance on 2004-03-17 under 510(k) number K033923. 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 TH0R DDII IR LAMP SYSTEM?

TH0R DDII IR LAMP SYSTEM is a medical device that received FDA 510(k) clearance on 2004-03-17. The listed applicant is Thor Intl.. The 510(k) number is K033923.

When did TH0R DDII IR LAMP SYSTEM receive FDA 510(k) clearance?

TH0R DDII IR LAMP SYSTEM received FDA 510(k) clearance on 2004-03-17, under 510(k) number K033923.

Who is the listed applicant for TH0R DDII IR LAMP SYSTEM?

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

What is the FDA product code for TH0R DDII IR LAMP SYSTEM?

The FDA product code for TH0R DDII IR LAMP SYSTEM is ILY.

Related Clinical Trials

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Other records listing Thor Intl. 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.

K030226THOR DDII 830CL3 LASER SYSTEM

Related Devices (Code: 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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