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FDA 510(k)

N-DEX

K-Number: K902696 · 1990-09-05

Decision Date1990-09-05
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

N-DEX is the device name listed in this FDA 510(k) record. The listed applicant is Moss Point Glove Co.. It received FDA 510(k) clearance on 1990-09-05 under 510(k) number K902696. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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