FDA 510(k)

SALUS - Hygiene Instrument Reprocessing Container

K-Number: K172292 · 2017-11-24

Decision Date2017-11-24

Product CodeKCT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SALUS - Hygiene Instrument Reprocessing Container is a medical device manufactured by Scican , Ltd.. It received FDA 510(k) clearance on 2017-11-24 under approval number K172292. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALUS - Hygiene Instrument Reprocessing Container?

SALUS - Hygiene Instrument Reprocessing Container is a medical device that received FDA 510(k) clearance on 2017-11-24. It is manufactured by Scican , Ltd.. The 510(k) number is K172292.

When was SALUS - Hygiene Instrument Reprocessing Container approved by the FDA?

SALUS - Hygiene Instrument Reprocessing Container received FDA 510(k) clearance on 2017-11-24, under approval number K172292.

What company makes SALUS - Hygiene Instrument Reprocessing Container?

SALUS - Hygiene Instrument Reprocessing Container is manufactured by Scican , Ltd..

What is the FDA product code for SALUS - Hygiene Instrument Reprocessing Container?

The FDA product code for SALUS - Hygiene Instrument Reprocessing Container is KCT.

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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.