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FDA 510(k)

SYNGO.PLAZA VB10A

K-Number: K132532 · 2013-12-09

ApplicantSiemens AG Healthcare
Decision Date2013-12-09
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO.PLAZA VB10A is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG Healthcare. It received FDA 510(k) clearance on 2013-12-09 under 510(k) number K132532. 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.PLAZA VB10A?

SYNGO.PLAZA VB10A is a medical device that received FDA 510(k) clearance on 2013-12-09. The listed applicant is Siemens AG Healthcare. The 510(k) number is K132532.

When did SYNGO.PLAZA VB10A receive FDA 510(k) clearance?

SYNGO.PLAZA VB10A received FDA 510(k) clearance on 2013-12-09, under 510(k) number K132532.

Who is the listed applicant for SYNGO.PLAZA VB10A?

The FDA 510(k) record lists Siemens AG Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNGO.PLAZA VB10A?

The FDA product code for SYNGO.PLAZA VB10A is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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