HARDYDISK AMOXICILLIN/CLAVULANIC ACID, 20/10MCG
K-Number: K003556 · 2001-01-17
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Device Summary
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.
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
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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