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FDA 510(k)

FREEPIX/PIXPACS DICOM/HTTP GATEWAY

K-Number: K970174 · 1997-05-01

ApplicantPixelinks, Inc.
Decision Date1997-05-01
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FREEPIX/PIXPACS DICOM/HTTP GATEWAY is the device name listed in this FDA 510(k) record. The listed applicant is Pixelinks, Inc.. It received FDA 510(k) clearance on 1997-05-01 under 510(k) number K970174. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEPIX/PIXPACS DICOM/HTTP GATEWAY?

FREEPIX/PIXPACS DICOM/HTTP GATEWAY is a medical device that received FDA 510(k) clearance on 1997-05-01. The listed applicant is Pixelinks, Inc.. The 510(k) number is K970174.

When did FREEPIX/PIXPACS DICOM/HTTP GATEWAY receive FDA 510(k) clearance?

FREEPIX/PIXPACS DICOM/HTTP GATEWAY received FDA 510(k) clearance on 1997-05-01, under 510(k) number K970174.

Who is the listed applicant for FREEPIX/PIXPACS DICOM/HTTP GATEWAY?

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

What is the FDA product code for FREEPIX/PIXPACS DICOM/HTTP GATEWAY?

The FDA product code for FREEPIX/PIXPACS DICOM/HTTP GATEWAY is LMD.

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Related Devices (Code: LMD)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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