N-DEX
K-Number: K902696 · 1990-09-05
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Device Summary
Frequently Asked Questions
What is the N-DEX?
N-DEX is a medical device that received FDA 510(k) clearance on 1990-09-05. The listed applicant is Moss Point Glove Co.. The 510(k) number is K902696.
When did N-DEX receive FDA 510(k) clearance?
N-DEX received FDA 510(k) clearance on 1990-09-05, under 510(k) number K902696.
Who is the listed applicant for N-DEX?
The FDA 510(k) record lists Moss Point Glove Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for N-DEX?
The FDA product code for N-DEX is LYY.
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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