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FDA 510(k)

LITEBOX DIAGNOSTIC REVIEW WORKSTATION

K-Number: K901158 · 1990-04-19

ApplicantSiemens Gammasonics, Inc.
Decision Date1990-04-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LITEBOX DIAGNOSTIC REVIEW WORKSTATION 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 1990-04-19 under 510(k) number K901158. 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 LITEBOX DIAGNOSTIC REVIEW WORKSTATION?

LITEBOX DIAGNOSTIC REVIEW WORKSTATION is a medical device that received FDA 510(k) clearance on 1990-04-19. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K901158.

When did LITEBOX DIAGNOSTIC REVIEW WORKSTATION receive FDA 510(k) clearance?

LITEBOX DIAGNOSTIC REVIEW WORKSTATION received FDA 510(k) clearance on 1990-04-19, under 510(k) number K901158.

Who is the listed applicant for LITEBOX DIAGNOSTIC REVIEW WORKSTATION?

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 LITEBOX DIAGNOSTIC REVIEW WORKSTATION?

The FDA product code for LITEBOX DIAGNOSTIC REVIEW WORKSTATION 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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