HARDY DISK AMPICILLIN/SULBACTAM
K-Number: K994067 · 2000-01-14
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Device Summary
Frequently Asked Questions
What is the HARDY DISK AMPICILLIN/SULBACTAM?
HARDY DISK AMPICILLIN/SULBACTAM is a medical device that received FDA 510(k) clearance on 2000-01-14. The listed applicant is Hardy Diagnostics. The 510(k) number is K994067.
When did HARDY DISK AMPICILLIN/SULBACTAM receive FDA 510(k) clearance?
HARDY DISK AMPICILLIN/SULBACTAM received FDA 510(k) clearance on 2000-01-14, under 510(k) number K994067.
Who is the listed applicant for HARDY DISK AMPICILLIN/SULBACTAM?
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 HARDY DISK AMPICILLIN/SULBACTAM?
The FDA product code for HARDY DISK AMPICILLIN/SULBACTAM 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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