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FDA 510(k)

POUR BOTTLE DECANTER #2010

K-Number: K823538 · 1983-01-26

ApplicantMedi-Plant Intl.
Decision Date1983-01-26
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POUR BOTTLE DECANTER #2010 is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Plant Intl.. It received FDA 510(k) clearance on 1983-01-26 under 510(k) number K823538. 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 POUR BOTTLE DECANTER #2010?

POUR BOTTLE DECANTER #2010 is a medical device that received FDA 510(k) clearance on 1983-01-26. The listed applicant is Medi-Plant Intl.. The 510(k) number is K823538.

When did POUR BOTTLE DECANTER #2010 receive FDA 510(k) clearance?

POUR BOTTLE DECANTER #2010 received FDA 510(k) clearance on 1983-01-26, under 510(k) number K823538.

Who is the listed applicant for POUR BOTTLE DECANTER #2010?

The FDA 510(k) record lists Medi-Plant Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POUR BOTTLE DECANTER #2010?

The FDA product code for POUR BOTTLE DECANTER #2010 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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