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FDA 510(k)

SIRSCAN

K-Number: K991473 · 1999-11-23

ApplicantIntelligence Artificielle Applications
Decision Date1999-11-23
Product CodeKZK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SIRSCAN is the device name listed in this FDA 510(k) record. The listed applicant is Intelligence Artificielle Applications. It received FDA 510(k) clearance on 1999-11-23 under 510(k) number K991473. The device is classified under product code KZK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIRSCAN?

SIRSCAN is a medical device that received FDA 510(k) clearance on 1999-11-23. The listed applicant is Intelligence Artificielle Applications. The 510(k) number is K991473.

When did SIRSCAN receive FDA 510(k) clearance?

SIRSCAN received FDA 510(k) clearance on 1999-11-23, under 510(k) number K991473.

Who is the listed applicant for SIRSCAN?

The FDA 510(k) record lists Intelligence Artificielle Applications as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIRSCAN?

The FDA product code for SIRSCAN is KZK.

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Related Devices (Code: KZK)

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.

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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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