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FDA 510(k)

SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE

K-Number: K935694 · 1994-03-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-03-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE 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 1994-03-07 under 510(k) number K935694. 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 SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE?

SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K935694.

When did SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE receive FDA 510(k) clearance?

SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE received FDA 510(k) clearance on 1994-03-07, under 510(k) number K935694.

Who is the listed applicant for SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE?

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 SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE?

The FDA product code for SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE is LLZ.

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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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