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FDA 510(k)

ULTRAPAK NEHA

K-Number: K010070 · 2001-03-15

ApplicantUltradent Products, Inc.
Decision Date2001-03-15
Product CodeMVL
DecisionSubstantially Equivalent

Device Summary

ULTRAPAK NEHA 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 2001-03-15 under 510(k) number K010070. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAPAK NEHA?

ULTRAPAK NEHA is a medical device that received FDA 510(k) clearance on 2001-03-15. The listed applicant is Ultradent Products, Inc.. The 510(k) number is K010070.

When did ULTRAPAK NEHA receive FDA 510(k) clearance?

ULTRAPAK NEHA received FDA 510(k) clearance on 2001-03-15, under 510(k) number K010070.

Who is the listed applicant for ULTRAPAK NEHA?

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 ULTRAPAK NEHA?

The FDA product code for ULTRAPAK NEHA is MVL.

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Related Devices (Code: MVL)

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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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