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FDA 510(k)

ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3

K-Number: K990442 · 1999-05-11

ApplicantVital Images, Inc.
Decision Date1999-05-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3 is the device name listed in this FDA 510(k) record. The listed applicant is Vital Images, Inc.. It received FDA 510(k) clearance on 1999-05-11 under 510(k) number K990442. 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 ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3?

ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3 is a medical device that received FDA 510(k) clearance on 1999-05-11. The listed applicant is Vital Images, Inc.. The 510(k) number is K990442.

When did ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3 receive FDA 510(k) clearance?

ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3 received FDA 510(k) clearance on 1999-05-11, under 510(k) number K990442.

Who is the listed applicant for ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3?

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

What is the FDA product code for ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3?

The FDA product code for ADVANCED DIAGNOSTIC VIEWER (AOX), MODEL VITRED 1.3 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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