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FDA 510(k)

HARDYDISK TRIMETHOPRIM 5MCG

K-Number: K003554 · 2001-01-19

Decision Date2001-01-19
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HARDYDISK TRIMETHOPRIM 5MCG is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Diagnostics. It received FDA 510(k) clearance on 2001-01-19 under 510(k) number K003554. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HARDYDISK TRIMETHOPRIM 5MCG?

HARDYDISK TRIMETHOPRIM 5MCG is a medical device that received FDA 510(k) clearance on 2001-01-19. The listed applicant is Hardy Diagnostics. The 510(k) number is K003554.

When did HARDYDISK TRIMETHOPRIM 5MCG receive FDA 510(k) clearance?

HARDYDISK TRIMETHOPRIM 5MCG received FDA 510(k) clearance on 2001-01-19, under 510(k) number K003554.

Who is the listed applicant for HARDYDISK TRIMETHOPRIM 5MCG?

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 HARDYDISK TRIMETHOPRIM 5MCG?

The FDA product code for HARDYDISK TRIMETHOPRIM 5MCG is JTN.

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 Hardy Diagnostics 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.

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Related Devices (Code: JTN)

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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