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FDA 510(k)

AX WORKSTATION DR-VIEWER SOFTWARE OPTION

K-Number: K992925 · 1999-11-23

ApplicantSiemens Corp.
Decision Date1999-11-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AX WORKSTATION DR-VIEWER SOFTWARE OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1999-11-23 under 510(k) number K992925. 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 AX WORKSTATION DR-VIEWER SOFTWARE OPTION?

AX WORKSTATION DR-VIEWER SOFTWARE OPTION is a medical device that received FDA 510(k) clearance on 1999-11-23. The listed applicant is Siemens Corp.. The 510(k) number is K992925.

When did AX WORKSTATION DR-VIEWER SOFTWARE OPTION receive FDA 510(k) clearance?

AX WORKSTATION DR-VIEWER SOFTWARE OPTION received FDA 510(k) clearance on 1999-11-23, under 510(k) number K992925.

Who is the listed applicant for AX WORKSTATION DR-VIEWER SOFTWARE OPTION?

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

What is the FDA product code for AX WORKSTATION DR-VIEWER SOFTWARE OPTION?

The FDA product code for AX WORKSTATION DR-VIEWER SOFTWARE OPTION 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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