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FDA 510(k)

SC 6000/ SC 6000P/ R50

K-Number: K944350 · 1995-04-10

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-04-10
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SC 6000/ SC 6000P/ R50 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 1995-04-10 under 510(k) number K944350. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SC 6000/ SC 6000P/ R50?

SC 6000/ SC 6000P/ R50 is a medical device that received FDA 510(k) clearance on 1995-04-10. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K944350.

When did SC 6000/ SC 6000P/ R50 receive FDA 510(k) clearance?

SC 6000/ SC 6000P/ R50 received FDA 510(k) clearance on 1995-04-10, under 510(k) number K944350.

Who is the listed applicant for SC 6000/ SC 6000P/ R50?

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 SC 6000/ SC 6000P/ R50?

The FDA product code for SC 6000/ SC 6000P/ R50 is DSI.

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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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