SOMATOM Drive
K号: K161196 · 2016-08-24
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器械摘要
SOMATOM Drive 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 2016-08-24 under 510(k) number K161196. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SOMATOM Drive?
SOMATOM Drive is a medical device that received FDA 510(k) clearance on 2016-08-24. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K161196.
When did SOMATOM Drive receive FDA 510(k) clearance?
SOMATOM Drive received FDA 510(k) clearance on 2016-08-24, under 510(k) number K161196.
Who is the listed applicant for SOMATOM Drive?
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 SOMATOM Drive?
The FDA product code for SOMATOM Drive is JAK.
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列明Siemens Medical Solutions USA, Inc.为申报人的其他记录
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官方来源
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