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FDA 510(k)

SPOTTEST NITRATE REAGENT A

K-Number: K840579 · 1984-02-27

Decision Date1984-02-27
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SPOTTEST NITRATE REAGENT A is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1984-02-27 under 510(k) number K840579. 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 SPOTTEST NITRATE REAGENT A?

SPOTTEST NITRATE REAGENT A is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K840579.

When did SPOTTEST NITRATE REAGENT A receive FDA 510(k) clearance?

SPOTTEST NITRATE REAGENT A received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840579.

Who is the listed applicant for SPOTTEST NITRATE REAGENT A?

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

What is the FDA product code for SPOTTEST NITRATE REAGENT A?

The FDA product code for SPOTTEST NITRATE REAGENT A 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 Difco Laboratories, 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 121 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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