CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS
K-Number: K070542 · 2007-03-23
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Device Summary
Frequently Asked Questions
What is the CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS?
CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS is a medical device that received FDA 510(k) clearance on 2007-03-23. The listed applicant is Digirad Corp.. The 510(k) number is K070542.
When did CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS receive FDA 510(k) clearance?
CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS received FDA 510(k) clearance on 2007-03-23, under 510(k) number K070542.
Who is the listed applicant for CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS?
The FDA 510(k) record lists Digirad Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS?
The FDA product code for CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS 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.
Other records listing Digirad 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: 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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