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FDA 510(k)

BIRTCHER UV LAMP

K-Number: K973865 · 1999-02-26

ApplicantMedfaxx, Inc.
Decision Date1999-02-26
Product CodeMXG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIRTCHER UV LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Medfaxx, Inc.. It received FDA 510(k) clearance on 1999-02-26 under 510(k) number K973865. The device is classified under product code MXG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIRTCHER UV LAMP?

BIRTCHER UV LAMP is a medical device that received FDA 510(k) clearance on 1999-02-26. The listed applicant is Medfaxx, Inc.. The 510(k) number is K973865.

When did BIRTCHER UV LAMP receive FDA 510(k) clearance?

BIRTCHER UV LAMP received FDA 510(k) clearance on 1999-02-26, under 510(k) number K973865.

Who is the listed applicant for BIRTCHER UV LAMP?

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

What is the FDA product code for BIRTCHER UV LAMP?

The FDA product code for BIRTCHER UV LAMP is MXG.

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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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