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FDA 510(k)

AMICAS WEB/INTRANET IMAGE SERVER

K-Number: K970064 · 1997-03-17

Decision Date1997-03-17
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AMICAS WEB/INTRANET IMAGE SERVER is the device name listed in this FDA 510(k) record. The listed applicant is Autocyt Group, Inc.. It received FDA 510(k) clearance on 1997-03-17 under 510(k) number K970064. 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 AMICAS WEB/INTRANET IMAGE SERVER?

AMICAS WEB/INTRANET IMAGE SERVER is a medical device that received FDA 510(k) clearance on 1997-03-17. The listed applicant is Autocyt Group, Inc.. The 510(k) number is K970064.

When did AMICAS WEB/INTRANET IMAGE SERVER receive FDA 510(k) clearance?

AMICAS WEB/INTRANET IMAGE SERVER received FDA 510(k) clearance on 1997-03-17, under 510(k) number K970064.

Who is the listed applicant for AMICAS WEB/INTRANET IMAGE SERVER?

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

What is the FDA product code for AMICAS WEB/INTRANET IMAGE SERVER?

The FDA product code for AMICAS WEB/INTRANET IMAGE SERVER is LMD.

Related Clinical Trials

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.

Related Devices (Code: LMD)

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.

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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