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FDA 510(k)

LIASYS 450

K-Number: K113131 · 2012-03-08

ApplicantAms
Decision Date2012-03-08
Product CodeCFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIASYS 450 is the device name listed in this FDA 510(k) record. The listed applicant is Ams. It received FDA 510(k) clearance on 2012-03-08 under 510(k) number K113131. The device is classified under product code CFR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIASYS 450?

LIASYS 450 is a medical device that received FDA 510(k) clearance on 2012-03-08. The listed applicant is Ams. The 510(k) number is K113131.

When did LIASYS 450 receive FDA 510(k) clearance?

LIASYS 450 received FDA 510(k) clearance on 2012-03-08, under 510(k) number K113131.

Who is the listed applicant for LIASYS 450?

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

What is the FDA product code for LIASYS 450?

The FDA product code for LIASYS 450 is CFR.

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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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