HARDYDISK AST DORIPENEM 10 UG
K-Number: K080019 · 2008-01-29
Advertisement
Device Summary
Frequently Asked Questions
What is the HARDYDISK AST DORIPENEM 10 UG?
HARDYDISK AST DORIPENEM 10 UG is a medical device that received FDA 510(k) clearance on 2008-01-29. The listed applicant is Hardy Diagnostics. The 510(k) number is K080019.
When did HARDYDISK AST DORIPENEM 10 UG receive FDA 510(k) clearance?
HARDYDISK AST DORIPENEM 10 UG received FDA 510(k) clearance on 2008-01-29, under 510(k) number K080019.
Who is the listed applicant for HARDYDISK AST DORIPENEM 10 UG?
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 AST DORIPENEM 10 UG?
The FDA product code for HARDYDISK AST DORIPENEM 10 UG 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.
Advertisement