IIVS INTEGRATED IMAGE VIEWING STATION
K-Number: K994329 · 2000-05-26
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Device Summary
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.
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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