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FDA 510(k)

VESISCAN

K-Number: K093485 · 2010-03-16

ApplicantLife-Tech, Inc.
Decision Date2010-03-16
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VESISCAN is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech, Inc.. It received FDA 510(k) clearance on 2010-03-16 under 510(k) number K093485. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESISCAN?

VESISCAN is a medical device that received FDA 510(k) clearance on 2010-03-16. The listed applicant is Life-Tech, Inc.. The 510(k) number is K093485.

When did VESISCAN receive FDA 510(k) clearance?

VESISCAN received FDA 510(k) clearance on 2010-03-16, under 510(k) number K093485.

Who is the listed applicant for VESISCAN?

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

What is the FDA product code for VESISCAN?

The FDA product code for VESISCAN is IYO.

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Other records listing Life-Tech, Inc. as applicant

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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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