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FDA 510(k)

NAKAO SNARE II AND NAKAO SNARE III

K-Number: K020891 · 2002-06-17

ApplicantGranit Medical Innovations
Decision Date2002-06-17
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NAKAO SNARE II AND NAKAO SNARE III is the device name listed in this FDA 510(k) record. The listed applicant is Granit Medical Innovations. It received FDA 510(k) clearance on 2002-06-17 under 510(k) number K020891. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAKAO SNARE II AND NAKAO SNARE III?

NAKAO SNARE II AND NAKAO SNARE III is a medical device that received FDA 510(k) clearance on 2002-06-17. The listed applicant is Granit Medical Innovations. The 510(k) number is K020891.

When did NAKAO SNARE II AND NAKAO SNARE III receive FDA 510(k) clearance?

NAKAO SNARE II AND NAKAO SNARE III received FDA 510(k) clearance on 2002-06-17, under 510(k) number K020891.

Who is the listed applicant for NAKAO SNARE II AND NAKAO SNARE III?

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

What is the FDA product code for NAKAO SNARE II AND NAKAO SNARE III?

The FDA product code for NAKAO SNARE II AND NAKAO SNARE III is FDI.

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Related Devices (Code: FDI)

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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.

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