CONMED LINVATEC 300W XENON LIGHT SOURCE
K-Number: K070376 · 2007-08-20
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Device Summary
Frequently Asked Questions
What is the CONMED LINVATEC 300W XENON LIGHT SOURCE?
CONMED LINVATEC 300W XENON LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 2007-08-20. The listed applicant is Conmed Linvatec. The 510(k) number is K070376.
When did CONMED LINVATEC 300W XENON LIGHT SOURCE receive FDA 510(k) clearance?
CONMED LINVATEC 300W XENON LIGHT SOURCE received FDA 510(k) clearance on 2007-08-20, under 510(k) number K070376.
Who is the listed applicant for CONMED LINVATEC 300W XENON LIGHT SOURCE?
The FDA 510(k) record lists Conmed Linvatec as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONMED LINVATEC 300W XENON LIGHT SOURCE?
The FDA product code for CONMED LINVATEC 300W XENON LIGHT SOURCE is GCT.
Related Clinical Trials
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.
Other records listing Conmed Linvatec 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.
Related Devices (Code: GCT)
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.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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