HERITAGE 10
K-Number: K924293 · 1993-05-26
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Device Summary
Frequently Asked Questions
What is the HERITAGE 10?
HERITAGE 10 is a medical device that received FDA 510(k) clearance on 1993-05-26. The listed applicant is Tjn Manufacturing,Inc.. The 510(k) number is K924293.
When did HERITAGE 10 receive FDA 510(k) clearance?
HERITAGE 10 received FDA 510(k) clearance on 1993-05-26, under 510(k) number K924293.
Who is the listed applicant for HERITAGE 10?
The FDA 510(k) record lists Tjn Manufacturing,Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HERITAGE 10?
The FDA product code for HERITAGE 10 is JFB.
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 Tjn Manufacturing,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: JFB)
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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