ACCU-BEAM 300W XENON LIGHT SOURCE
K-Number: K951895 · 1995-05-24
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Device Summary
Frequently Asked Questions
What is the ACCU-BEAM 300W XENON LIGHT SOURCE?
ACCU-BEAM 300W XENON LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Tti Medical. The 510(k) number is K951895.
When did ACCU-BEAM 300W XENON LIGHT SOURCE receive FDA 510(k) clearance?
ACCU-BEAM 300W XENON LIGHT SOURCE received FDA 510(k) clearance on 1995-05-24, under 510(k) number K951895.
Who is the listed applicant for ACCU-BEAM 300W XENON LIGHT SOURCE?
The FDA 510(k) record lists Tti Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCU-BEAM 300W XENON LIGHT SOURCE?
The FDA product code for ACCU-BEAM 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 Tti Medical 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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