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FDA 510(k)

DENTA PORT

K-Number: K022147 · 2002-12-20

ApplicantJ. Morita USA, Inc.
Decision Date2002-12-20
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

DENTA PORT is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2002-12-20 under 510(k) number K022147. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTA PORT?

DENTA PORT is a medical device that received FDA 510(k) clearance on 2002-12-20. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K022147.

When did DENTA PORT receive FDA 510(k) clearance?

DENTA PORT received FDA 510(k) clearance on 2002-12-20, under 510(k) number K022147.

Who is the listed applicant for DENTA PORT?

The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTA PORT?

The FDA product code for DENTA PORT is LQY.

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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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