FDA 510(k)

NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC

K-Number: K930536 · 1994-12-15

Decision Date1994-12-15

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC is the device name listed in this FDA 510(k) record. The listed applicant is Neuromed, Inc.. It received FDA 510(k) clearance on 1994-12-15 under 510(k) number K930536. 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 OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC?

NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Neuromed, Inc.. The 510(k) number is K930536.

When did NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC receive FDA 510(k) clearance?

NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC received FDA 510(k) clearance on 1994-12-15, under 510(k) number K930536.

Who is the listed applicant for NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC?

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 OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC?

The FDA product code for NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC is GZB.

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Other records listing Neuromed, Inc. as applicant

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Related Devices (Code: GZB)

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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.