LEGACY-XT
K-Number: K922451 · 1992-08-05
Advertisement
Device Summary
Frequently Asked Questions
What is the LEGACY-XT?
LEGACY-XT is a medical device that received FDA 510(k) clearance on 1992-08-05. The listed applicant is J.F. Jelenko & Co., Inc.. The 510(k) number is K922451.
When did LEGACY-XT receive FDA 510(k) clearance?
LEGACY-XT received FDA 510(k) clearance on 1992-08-05, under 510(k) number K922451.
Who is the listed applicant for LEGACY-XT?
The FDA 510(k) record lists J.F. Jelenko & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEGACY-XT?
The FDA product code for LEGACY-XT is EJS.
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 J.F. Jelenko & Co., Inc. 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: EJS)
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