JAI
K-Number: K951513 · 1995-05-25
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Device Summary
Frequently Asked Questions
What is the JAI?
JAI is a medical device that received FDA 510(k) clearance on 1995-05-25. The listed applicant is Intl. Trade Management Co.. The 510(k) number is K951513.
When did JAI receive FDA 510(k) clearance?
JAI received FDA 510(k) clearance on 1995-05-25, under 510(k) number K951513.
Who is the listed applicant for JAI?
The FDA 510(k) record lists Intl. Trade Management Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JAI?
The FDA product code for JAI is LYY.
Other records listing Intl. Trade Management Co. 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: LYY)
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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