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FDA 510(k)

STA LIATEST FREE PS

K-Number: K092170 · 2009-12-22

ApplicantDiagnostica Stago, Inc.
Decision Date2009-12-22
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

STA LIATEST FREE PS is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostica Stago, Inc.. It received FDA 510(k) clearance on 2009-12-22 under 510(k) number K092170. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STA LIATEST FREE PS?

STA LIATEST FREE PS is a medical device that received FDA 510(k) clearance on 2009-12-22. The listed applicant is Diagnostica Stago, Inc.. The 510(k) number is K092170.

When did STA LIATEST FREE PS receive FDA 510(k) clearance?

STA LIATEST FREE PS received FDA 510(k) clearance on 2009-12-22, under 510(k) number K092170.

Who is the listed applicant for STA LIATEST FREE PS?

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

What is the FDA product code for STA LIATEST FREE PS?

The FDA product code for STA LIATEST FREE PS is GGP.

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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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