ACCU-BEAM YAG FIBER
K-Number: K890922 · 1989-05-15
Advertisement
Device Summary
Frequently Asked Questions
What is the ACCU-BEAM YAG FIBER?
ACCU-BEAM YAG FIBER is a medical device that received FDA 510(k) clearance on 1989-05-15. The listed applicant is Tti Medical. The 510(k) number is K890922.
When did ACCU-BEAM YAG FIBER receive FDA 510(k) clearance?
ACCU-BEAM YAG FIBER received FDA 510(k) clearance on 1989-05-15, under 510(k) number K890922.
Who is the listed applicant for ACCU-BEAM YAG FIBER?
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 YAG FIBER?
The FDA product code for ACCU-BEAM YAG FIBER 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.
Advertisement