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FDA 510(k)

SIENET DIAGNOSTIC REPORTING CONSOLE

K-Number: K920309 · 1992-03-20

ApplicantSiemens Gammasonics, Inc.
Decision Date1992-03-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIENET DIAGNOSTIC REPORTING CONSOLE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Gammasonics, Inc.. It received FDA 510(k) clearance on 1992-03-20 under 510(k) number K920309. 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?

SIENET DIAGNOSTIC REPORTING CONSOLE is a medical device that received FDA 510(k) clearance on 1992-03-20. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K920309.

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

SIENET DIAGNOSTIC REPORTING CONSOLE received FDA 510(k) clearance on 1992-03-20, under 510(k) number K920309.

Who is the listed applicant for SIENET DIAGNOSTIC REPORTING CONSOLE?

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

What is the FDA product code for SIENET DIAGNOSTIC REPORTING CONSOLE?

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

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Other records listing Siemens Gammasonics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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