FDA 510(k)

SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900

K-Nummer: K230582 · 2023-03-28

Entscheidungsdatum2023-03-28

ProduktcodeMED

BeratungsausschussHO

EntscheidungSubstantially Equivalent

Produktübersicht

SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900 is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2023-03-28 under 510(k) number K230582. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900?

SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900 is a medical device that received FDA 510(k) clearance on 2023-03-28. The listed applicant is STERIS Corporation. The 510(k) number is K230582.

When did SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900 receive FDA 510(k) clearance?

SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900 received FDA 510(k) clearance on 2023-03-28, under 510(k) number K230582.

Who is the listed applicant for SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900?

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

What is the FDA product code for SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900?

The FDA product code for SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900 is MED.

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Weitere Einträge mit STERIS Corporation als Antragsteller

K261055AMSCO 700 Dampfsterilisator K260766Celerity 5 HP Biological Indicator (LCB052)K251666SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700; SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900 K252680Celerity™ 20 HP Biological Indicator K251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118 K243876VERIFY STEAM Integrating Indicator

Alle 120 Geräte anzeigen →

Verwandte Geräte (Code: MED)

Offizielle Quelle

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