EMISSION TOMOGRAPHY CAROUSEL
K-Number: K896151 · 1991-04-16
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Device Summary
Frequently Asked Questions
What is the EMISSION TOMOGRAPHY CAROUSEL?
EMISSION TOMOGRAPHY CAROUSEL is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is Atf Consolidated. The 510(k) number is K896151.
When did EMISSION TOMOGRAPHY CAROUSEL receive FDA 510(k) clearance?
EMISSION TOMOGRAPHY CAROUSEL received FDA 510(k) clearance on 1991-04-16, under 510(k) number K896151.
Who is the listed applicant for EMISSION TOMOGRAPHY CAROUSEL?
The FDA 510(k) record lists Atf Consolidated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMISSION TOMOGRAPHY CAROUSEL?
The FDA product code for EMISSION TOMOGRAPHY CAROUSEL is KPS.
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.
Related Devices (Code: KPS)
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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