CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY
K-Number: K882271 · 1988-11-03
Advertisement
Device Summary
Frequently Asked Questions
What is the CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY?
CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY is a medical device that received FDA 510(k) clearance on 1988-11-03. The listed applicant is Nuccardiac Software, Inc.. The 510(k) number is K882271.
When did CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY receive FDA 510(k) clearance?
CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY received FDA 510(k) clearance on 1988-11-03, under 510(k) number K882271.
Who is the listed applicant for CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY?
The FDA 510(k) record lists Nuccardiac Software, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY?
The FDA product code for CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY is LLZ.
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 Nuccardiac Software, Inc. 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: LLZ)
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