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FDA 510(k)

APOLLO IR HEAT LAMP SYSTEM

K-Number: K060134 · 2006-03-21

ApplicantApollo Physical Therapy Products International
Decision Date2006-03-21
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

APOLLO IR HEAT LAMP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Apollo Physical Therapy Products International. It received FDA 510(k) clearance on 2006-03-21 under 510(k) number K060134. 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 APOLLO IR HEAT LAMP SYSTEM?

APOLLO IR HEAT LAMP SYSTEM is a medical device that received FDA 510(k) clearance on 2006-03-21. The listed applicant is Apollo Physical Therapy Products International. The 510(k) number is K060134.

When did APOLLO IR HEAT LAMP SYSTEM receive FDA 510(k) clearance?

APOLLO IR HEAT LAMP SYSTEM received FDA 510(k) clearance on 2006-03-21, under 510(k) number K060134.

Who is the listed applicant for APOLLO IR HEAT LAMP SYSTEM?

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

What is the FDA product code for APOLLO IR HEAT LAMP SYSTEM?

The FDA product code for APOLLO IR HEAT LAMP SYSTEM 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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