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FDA 510(k)

SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER

K-Number: K970348 · 1997-08-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1997-08-15
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER 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 1997-08-15 under 510(k) number K970348. 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 SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER?

SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER is a medical device that received FDA 510(k) clearance on 1997-08-15. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K970348.

When did SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER receive FDA 510(k) clearance?

SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER received FDA 510(k) clearance on 1997-08-15, under 510(k) number K970348.

Who is the listed applicant for SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER?

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 SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER?

The FDA product code for SIEMENS SC/9000/SC9015 SERIES SURGICAL DISPLAY CONTROLLER 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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