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FDA 510(k)

NITRATE REAGENTS A, B AND C

K-Number: K930717 · 1993-04-23

ApplicantHardy Diagnostics
Decision Date1993-04-23
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NITRATE REAGENTS A, B AND C is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Diagnostics. It received FDA 510(k) clearance on 1993-04-23 under 510(k) number K930717. 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 NITRATE REAGENTS A, B AND C?

NITRATE REAGENTS A, B AND C is a medical device that received FDA 510(k) clearance on 1993-04-23. The listed applicant is Hardy Diagnostics. The 510(k) number is K930717.

When did NITRATE REAGENTS A, B AND C receive FDA 510(k) clearance?

NITRATE REAGENTS A, B AND C received FDA 510(k) clearance on 1993-04-23, under 510(k) number K930717.

Who is the listed applicant for NITRATE REAGENTS A, B AND C?

The FDA 510(k) record lists Hardy Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NITRATE REAGENTS A, B AND C?

The FDA product code for NITRATE REAGENTS A, B AND C is JTO.

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Related Devices (Code: 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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