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FDA 510(k)

SALUS - Hygiene Instrument Reprocessing Container

K-Number: K172292 · 2017-11-24

ApplicantScican , Ltd.
Decision Date2017-11-24
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SALUS - Hygiene Instrument Reprocessing Container is the device name listed in this FDA 510(k) record. The listed applicant is Scican , Ltd.. It received FDA 510(k) clearance on 2017-11-24 under 510(k) 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. The listed applicant is Scican , Ltd.. The 510(k) number is K172292.

When did SALUS - Hygiene Instrument Reprocessing Container receive FDA 510(k) clearance?

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

Who is the listed applicant for SALUS - Hygiene Instrument Reprocessing Container?

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

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

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

Other records listing Scican , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: KCT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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