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FDA 510(k)

QUIET/SILENT SCANNING SUITE

K-Number: K132831 · 2013-11-01

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2013-11-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QUIET/SILENT SCANNING SUITE 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 2013-11-01 under 510(k) number K132831. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIET/SILENT SCANNING SUITE?

QUIET/SILENT SCANNING SUITE is a medical device that received FDA 510(k) clearance on 2013-11-01. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K132831.

When did QUIET/SILENT SCANNING SUITE receive FDA 510(k) clearance?

QUIET/SILENT SCANNING SUITE received FDA 510(k) clearance on 2013-11-01, under 510(k) number K132831.

Who is the listed applicant for QUIET/SILENT SCANNING SUITE?

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 QUIET/SILENT SCANNING SUITE?

The FDA product code for QUIET/SILENT SCANNING SUITE is LNH.

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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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