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FDA 510(k)

SYNGO NEURO PBV-IR

K-Number: K111052 · 2011-05-20

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2011-05-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO NEURO PBV-IR 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 2011-05-20 under 510(k) number K111052. 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 SYNGO NEURO PBV-IR?

SYNGO NEURO PBV-IR is a medical device that received FDA 510(k) clearance on 2011-05-20. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K111052.

When did SYNGO NEURO PBV-IR receive FDA 510(k) clearance?

SYNGO NEURO PBV-IR received FDA 510(k) clearance on 2011-05-20, under 510(k) number K111052.

Who is the listed applicant for SYNGO NEURO PBV-IR?

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 SYNGO NEURO PBV-IR?

The FDA product code for SYNGO NEURO PBV-IR 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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