Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY

K-Number: K882271 · 1988-11-03

Decision Date1988-11-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CTQ - CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALY is the device name listed in this FDA 510(k) record. The listed applicant is Nuccardiac Software, Inc.. It received FDA 510(k) clearance on 1988-11-03 under 510(k) number K882271. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 12 devices →

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.

↑