HIPPURATE TEST DISKS
K-Number: K842868 · 1984-08-03
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Device Summary
Frequently Asked Questions
What is the HIPPURATE TEST DISKS?
HIPPURATE TEST DISKS is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is Irvine Diagnostic Services. The 510(k) number is K842868.
When did HIPPURATE TEST DISKS receive FDA 510(k) clearance?
HIPPURATE TEST DISKS received FDA 510(k) clearance on 1984-08-03, under 510(k) number K842868.
Who is the listed applicant for HIPPURATE TEST DISKS?
The FDA 510(k) record lists Irvine Diagnostic Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIPPURATE TEST DISKS?
The FDA product code for HIPPURATE TEST DISKS is JSF.
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 Irvine Diagnostic Services 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: JSF)
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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