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FDA 510(k)

LXN FRUCTOSAMINE TEST

K-Number: K955629 · 1996-03-20

ApplicantLxn Corp.
Decision Date1996-03-20
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LXN FRUCTOSAMINE TEST is the device name listed in this FDA 510(k) record. The listed applicant is Lxn Corp.. It received FDA 510(k) clearance on 1996-03-20 under 510(k) number K955629. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LXN FRUCTOSAMINE TEST?

LXN FRUCTOSAMINE TEST is a medical device that received FDA 510(k) clearance on 1996-03-20. The listed applicant is Lxn Corp.. The 510(k) number is K955629.

When did LXN FRUCTOSAMINE TEST receive FDA 510(k) clearance?

LXN FRUCTOSAMINE TEST received FDA 510(k) clearance on 1996-03-20, under 510(k) number K955629.

Who is the listed applicant for LXN FRUCTOSAMINE TEST?

The FDA 510(k) record lists Lxn Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LXN FRUCTOSAMINE TEST?

The FDA product code for LXN FRUCTOSAMINE TEST is JJX.

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Other records listing Lxn Corp. 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.

K002688PERSONAL GLUCOSE CONTROL CHARTING SYSTEMK991754GO GLUCOSE MONITORING SYSTEMK990942DUET II GLUCOSE CONTROL MONITORING SYSTEMK973140DUET GLUCOSE CONTROL MONITORING SYSTEMK962597LXN FRUCTOSAMINE TEST SYSTEMK960034LXN BLOOD GLUCOSE TEST SYSTEM

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Related Devices (Code: JJX)

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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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