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FDA 510(k)

SANDMAN POCKET

K-Number: K061996 · 2006-10-03

ApplicantEb Neuro S.P.A.
Decision Date2006-10-03
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SANDMAN POCKET is the device name listed in this FDA 510(k) record. The listed applicant is Eb Neuro S.P.A.. It received FDA 510(k) clearance on 2006-10-03 under 510(k) number K061996. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SANDMAN POCKET?

SANDMAN POCKET is a medical device that received FDA 510(k) clearance on 2006-10-03. The listed applicant is Eb Neuro S.P.A.. The 510(k) number is K061996.

When did SANDMAN POCKET receive FDA 510(k) clearance?

SANDMAN POCKET received FDA 510(k) clearance on 2006-10-03, under 510(k) number K061996.

Who is the listed applicant for SANDMAN POCKET?

The FDA 510(k) record lists Eb Neuro S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SANDMAN POCKET?

The FDA product code for SANDMAN POCKET is MNR.

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Other records listing Eb Neuro S.P.A. as applicant

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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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