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FDA 510(k)

NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735

K-Number: K021196 · 2002-07-01

Decision Date2002-07-01
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735 is the device name listed in this FDA 510(k) record. The listed applicant is Neuron Therapeutics, Inc.. It received FDA 510(k) clearance on 2002-07-01 under 510(k) number K021196. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735?

NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735 is a medical device that received FDA 510(k) clearance on 2002-07-01. The listed applicant is Neuron Therapeutics, Inc.. The 510(k) number is K021196.

When did NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735 receive FDA 510(k) clearance?

NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735 received FDA 510(k) clearance on 2002-07-01, under 510(k) number K021196.

Who is the listed applicant for NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735?

The FDA 510(k) record lists Neuron Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735?

The FDA product code for NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735 is JXG.

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.

Related Devices (Code: JXG)

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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