OLYMPUS GGT REAGENT
K-Number: K922230 · 1992-06-25
Advertisement
Device Summary
Frequently Asked Questions
What is the OLYMPUS GGT REAGENT?
OLYMPUS GGT REAGENT is a medical device that received FDA 510(k) clearance on 1992-06-25. The listed applicant is Olympus Corp.. The 510(k) number is K922230.
When did OLYMPUS GGT REAGENT receive FDA 510(k) clearance?
OLYMPUS GGT REAGENT received FDA 510(k) clearance on 1992-06-25, under 510(k) number K922230.
Who is the listed applicant for OLYMPUS GGT REAGENT?
The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OLYMPUS GGT REAGENT?
The FDA product code for OLYMPUS GGT REAGENT is JQB.
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 Olympus Corp. 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: JQB)
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