PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE
K-Number: K982536 · 1998-11-24
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Device Summary
Frequently Asked Questions
What is the PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE?
PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE is a medical device that received FDA 510(k) clearance on 1998-11-24. The listed applicant is Siemens Corp.. The 510(k) number is K982536.
When did PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE receive FDA 510(k) clearance?
PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE received FDA 510(k) clearance on 1998-11-24, under 510(k) number K982536.
Who is the listed applicant for PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE?
The FDA 510(k) record lists Siemens Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE?
The FDA product code for PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE is JAK.
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 Siemens Corp. 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: JAK)
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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