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FDA 510(k)

MODULARIS VARIOSTAR

K-Number: K070799 · 2007-11-01

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2007-11-01
Product CodeLNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODULARIS VARIOSTAR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2007-11-01 under 510(k) number K070799. The device is classified under product code LNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULARIS VARIOSTAR?

MODULARIS VARIOSTAR is a medical device that received FDA 510(k) clearance on 2007-11-01. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K070799.

When did MODULARIS VARIOSTAR receive FDA 510(k) clearance?

MODULARIS VARIOSTAR received FDA 510(k) clearance on 2007-11-01, under 510(k) number K070799.

Who is the listed applicant for MODULARIS VARIOSTAR?

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

What is the FDA product code for MODULARIS VARIOSTAR?

The FDA product code for MODULARIS VARIOSTAR is LNS.

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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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