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FDA 510(k)

DECANTER MODELS-VARIOUS

K-Number: K830232 · 1983-02-09

ApplicantSteri-Sytems, Corp.
Decision Date1983-02-09
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DECANTER MODELS-VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Steri-Sytems, Corp.. It received FDA 510(k) clearance on 1983-02-09 under 510(k) number K830232. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DECANTER MODELS-VARIOUS?

DECANTER MODELS-VARIOUS is a medical device that received FDA 510(k) clearance on 1983-02-09. The listed applicant is Steri-Sytems, Corp.. The 510(k) number is K830232.

When did DECANTER MODELS-VARIOUS receive FDA 510(k) clearance?

DECANTER MODELS-VARIOUS received FDA 510(k) clearance on 1983-02-09, under 510(k) number K830232.

Who is the listed applicant for DECANTER MODELS-VARIOUS?

The FDA 510(k) record lists Steri-Sytems, Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DECANTER MODELS-VARIOUS?

The FDA product code for DECANTER MODELS-VARIOUS is KPE.

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Related Devices (Code: KPE)

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.

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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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