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FDA 510(k)

VARIOSURG

K-Number: K073678 · 2008-07-10

ApplicantNakanishi, Inc.
Decision Date2008-07-10
Product CodeDZI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VARIOSURG is the device name listed in this FDA 510(k) record. The listed applicant is Nakanishi, Inc.. It received FDA 510(k) clearance on 2008-07-10 under 510(k) number K073678. The device is classified under product code DZI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIOSURG?

VARIOSURG is a medical device that received FDA 510(k) clearance on 2008-07-10. The listed applicant is Nakanishi, Inc.. The 510(k) number is K073678.

When did VARIOSURG receive FDA 510(k) clearance?

VARIOSURG received FDA 510(k) clearance on 2008-07-10, under 510(k) number K073678.

Who is the listed applicant for VARIOSURG?

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

What is the FDA product code for VARIOSURG?

The FDA product code for VARIOSURG is DZI.

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Related Devices (Code: DZI)

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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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