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FDA 510(k)

CITRIC ACID 20% SOLUTION, MODEL 329

K-Number: K063703 · 2006-12-21

ApplicantUltradent Products, Inc.
Decision Date2006-12-21
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

CITRIC ACID 20% SOLUTION, MODEL 329 is the device name listed in this FDA 510(k) record. The listed applicant is Ultradent Products, Inc.. It received FDA 510(k) clearance on 2006-12-21 under 510(k) number K063703. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CITRIC ACID 20% SOLUTION, MODEL 329?

CITRIC ACID 20% SOLUTION, MODEL 329 is a medical device that received FDA 510(k) clearance on 2006-12-21. The listed applicant is Ultradent Products, Inc.. The 510(k) number is K063703.

When did CITRIC ACID 20% SOLUTION, MODEL 329 receive FDA 510(k) clearance?

CITRIC ACID 20% SOLUTION, MODEL 329 received FDA 510(k) clearance on 2006-12-21, under 510(k) number K063703.

Who is the listed applicant for CITRIC ACID 20% SOLUTION, MODEL 329?

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

What is the FDA product code for CITRIC ACID 20% SOLUTION, MODEL 329?

The FDA product code for CITRIC ACID 20% SOLUTION, MODEL 329 is KJJ.

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Related Devices (Code: KJJ)

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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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