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FDA 510(k)

NEUROMED MODEL 1992 LS LAMITRODE LEAD

K-Number: K905255 · 1991-01-25

ApplicantNeuromed, Inc.
Decision Date1991-01-25
Product CodeGZB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMED MODEL 1992 LS LAMITRODE LEAD is the device name listed in this FDA 510(k) record. The listed applicant is Neuromed, Inc.. It received FDA 510(k) clearance on 1991-01-25 under 510(k) number K905255. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMED MODEL 1992 LS LAMITRODE LEAD?

NEUROMED MODEL 1992 LS LAMITRODE LEAD is a medical device that received FDA 510(k) clearance on 1991-01-25. The listed applicant is Neuromed, Inc.. The 510(k) number is K905255.

When did NEUROMED MODEL 1992 LS LAMITRODE LEAD receive FDA 510(k) clearance?

NEUROMED MODEL 1992 LS LAMITRODE LEAD received FDA 510(k) clearance on 1991-01-25, under 510(k) number K905255.

Who is the listed applicant for NEUROMED MODEL 1992 LS LAMITRODE LEAD?

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

What is the FDA product code for NEUROMED MODEL 1992 LS LAMITRODE LEAD?

The FDA product code for NEUROMED MODEL 1992 LS LAMITRODE LEAD is GZB.

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Related Devices (Code: GZB)

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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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