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FDA 510(k)

HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG

K-Number: K003556 · 2001-01-17

Decision Date2001-01-17
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Diagnostics. It received FDA 510(k) clearance on 2001-01-17 under 510(k) number K003556. 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 AMOXICILLIN/CLAVULANIC ACID, 20/10MCG?

HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG is a medical device that received FDA 510(k) clearance on 2001-01-17. The listed applicant is Hardy Diagnostics. The 510(k) number is K003556.

When did HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG receive FDA 510(k) clearance?

HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG received FDA 510(k) clearance on 2001-01-17, under 510(k) number K003556.

Who is the listed applicant for HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG?

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 AMOXICILLIN/CLAVULANIC ACID, 20/10MCG?

The FDA product code for HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG 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.

View all 108 devices →

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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