Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DMAC INDOLE REAGENT

K-Number: K901390 · 1990-04-16

Decision Date1990-04-16
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DMAC INDOLE REAGENT 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 1990-04-16 under 510(k) number K901390. 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 DMAC INDOLE REAGENT?

DMAC INDOLE REAGENT is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Analytical Products, Inc.. The 510(k) number is K901390.

When did DMAC INDOLE REAGENT receive FDA 510(k) clearance?

DMAC INDOLE REAGENT received FDA 510(k) clearance on 1990-04-16, under 510(k) number K901390.

Who is the listed applicant for DMAC INDOLE REAGENT?

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 DMAC INDOLE REAGENT?

The FDA product code for DMAC INDOLE REAGENT is JTO.

Related Clinical Trials

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.

Other records listing Analytical Products, Inc. as applicant

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.

View all 57 devices →

Related Devices (Code: JTO)

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.

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.

↑