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FDA 510(k)

IIVS INTEGRATED IMAGE VIEWING STATION

K-Number: K994329 · 2000-05-26

Decision Date2000-05-26
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IIVS INTEGRATED IMAGE VIEWING STATION is the device name listed in this FDA 510(k) record. The listed applicant is Terarecon,Inc.. It received FDA 510(k) clearance on 2000-05-26 under 510(k) number K994329. 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 IIVS INTEGRATED IMAGE VIEWING STATION?

IIVS INTEGRATED IMAGE VIEWING STATION is a medical device that received FDA 510(k) clearance on 2000-05-26. The listed applicant is Terarecon,Inc.. The 510(k) number is K994329.

When did IIVS INTEGRATED IMAGE VIEWING STATION receive FDA 510(k) clearance?

IIVS INTEGRATED IMAGE VIEWING STATION received FDA 510(k) clearance on 2000-05-26, under 510(k) number K994329.

Who is the listed applicant for IIVS INTEGRATED IMAGE VIEWING STATION?

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

What is the FDA product code for IIVS INTEGRATED IMAGE VIEWING STATION?

The FDA product code for IIVS INTEGRATED IMAGE VIEWING STATION 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.

Other records listing Terarecon,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.

View all 14 devices →

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

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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