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FDA 510(k)

LIASYS WITH MODELS LIASYS

K-Number: K080468 · 2008-07-25

ApplicantAms S.R.L. Analyzer Medical System
Decision Date2008-07-25
Product CodeCFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIASYS WITH MODELS LIASYS is the device name listed in this FDA 510(k) record. The listed applicant is Ams S.R.L. Analyzer Medical System. It received FDA 510(k) clearance on 2008-07-25 under 510(k) number K080468. 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 WITH MODELS LIASYS?

LIASYS WITH MODELS LIASYS is a medical device that received FDA 510(k) clearance on 2008-07-25. The listed applicant is Ams S.R.L. Analyzer Medical System. The 510(k) number is K080468.

When did LIASYS WITH MODELS LIASYS receive FDA 510(k) clearance?

LIASYS WITH MODELS LIASYS received FDA 510(k) clearance on 2008-07-25, under 510(k) number K080468.

Who is the listed applicant for LIASYS WITH MODELS LIASYS?

The FDA 510(k) record lists Ams S.R.L. Analyzer Medical System as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIASYS WITH MODELS LIASYS?

The FDA product code for LIASYS WITH MODELS LIASYS 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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