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FDA 510(k)

IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0

K-Number: K022940 · 2002-10-11

ApplicantIntelligent Images Srl
Decision Date2002-10-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Intelligent Images Srl. It received FDA 510(k) clearance on 2002-10-11 under 510(k) number K022940. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0?

IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0 is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Intelligent Images Srl. The 510(k) number is K022940.

When did IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0 receive FDA 510(k) clearance?

IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0 received FDA 510(k) clearance on 2002-10-11, under 510(k) number K022940.

Who is the listed applicant for IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0?

The FDA 510(k) record lists Intelligent Images Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0?

The FDA product code for IN-VISION VIEW WITH MEASUREMENTS MODULE, MODEL 1.0 is LLZ.

Related Clinical Trials

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Other records listing Intelligent Images Srl 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.

K041581COMPACS, VERSION 1.0

Related Devices (Code: LLZ)

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

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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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