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FDA 510(k)

SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827

K-Number: K100619 · 2010-05-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2010-05-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827 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 2010-05-07 under 510(k) number K100619. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827?

SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827 is a medical device that received FDA 510(k) clearance on 2010-05-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K100619.

When did SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827 receive FDA 510(k) clearance?

SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827 received FDA 510(k) clearance on 2010-05-07, under 510(k) number K100619.

Who is the listed applicant for SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827?

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 SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827?

The FDA product code for SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827 is LLZ.

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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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