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FDA 510(k)

API ANAIDENT

K-Number: K831032 · 1983-05-05

ApplicantAnalytical Products, Inc.
Decision Date1983-05-05
Product CodeJSP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

API ANAIDENT 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 1983-05-05 under 510(k) number K831032. The device is classified under product code JSP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the API ANAIDENT?

API ANAIDENT is a medical device that received FDA 510(k) clearance on 1983-05-05. The listed applicant is Analytical Products, Inc.. The 510(k) number is K831032.

When did API ANAIDENT receive FDA 510(k) clearance?

API ANAIDENT received FDA 510(k) clearance on 1983-05-05, under 510(k) number K831032.

Who is the listed applicant for API ANAIDENT?

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 API ANAIDENT?

The FDA product code for API ANAIDENT is JSP.

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Other records listing Analytical Products, Inc. as applicant

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Related Devices (Code: JSP)

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

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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