SALUS - Hygiene Instrument Reprocessing Container
K-Number: K172292 · 2017-11-24
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.