ACCU-BEAM WAVEGUIDE
K-Number: K895656 · 1990-02-22
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Device Summary
Frequently Asked Questions
What is the ACCU-BEAM WAVEGUIDE?
ACCU-BEAM WAVEGUIDE is a medical device that received FDA 510(k) clearance on 1990-02-22. The listed applicant is Tti Medical. The 510(k) number is K895656.
When did ACCU-BEAM WAVEGUIDE receive FDA 510(k) clearance?
ACCU-BEAM WAVEGUIDE received FDA 510(k) clearance on 1990-02-22, under 510(k) number K895656.
Who is the listed applicant for ACCU-BEAM WAVEGUIDE?
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 WAVEGUIDE?
The FDA product code for ACCU-BEAM WAVEGUIDE is GEX. This falls under the Gastroenterology category.
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: GEX)
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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