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FDA 510(k)

INFRADIODE INFRARED LAMP

K-Number: K837517 · 1983-06-14

ApplicantPhimo of Texas, Inc.
Decision Date1983-06-14
Product Code
DecisionSubstantially Equivalent

Device Summary

INFRADIODE INFRARED LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Phimo of Texas, Inc.. It received FDA 510(k) clearance on 1983-06-14 under 510(k) number K837517. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFRADIODE INFRARED LAMP?

INFRADIODE INFRARED LAMP is a medical device that received FDA 510(k) clearance on 1983-06-14. The listed applicant is Phimo of Texas, Inc.. The 510(k) number is K837517.

When did INFRADIODE INFRARED LAMP receive FDA 510(k) clearance?

INFRADIODE INFRARED LAMP received FDA 510(k) clearance on 1983-06-14, under 510(k) number K837517.

Who is the listed applicant for INFRADIODE INFRARED LAMP?

The FDA 510(k) record lists Phimo of Texas, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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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