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FDA 510(k)

NEIDENT*

K-Number: K821907 · 1982-07-22

ApplicantAnalytical Products, Inc.
Decision Date1982-07-22
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NEIDENT* is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1982-07-22 under 510(k) number K821907. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEIDENT*?

NEIDENT* is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Analytical Products, Inc.. The 510(k) number is K821907.

When did NEIDENT* receive FDA 510(k) clearance?

NEIDENT* received FDA 510(k) clearance on 1982-07-22, under 510(k) number K821907.

Who is the listed applicant for NEIDENT*?

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

What is the FDA product code for NEIDENT*?

The FDA product code for NEIDENT* is JTO.

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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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