FLEXIBLE CARDIAC COIL
K-Number: K110487 · 2011-04-19
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Device Summary
Frequently Asked Questions
What is the FLEXIBLE CARDIAC COIL?
FLEXIBLE CARDIAC COIL is a medical device that received FDA 510(k) clearance on 2011-04-19. The listed applicant is Lbds Holding Company. The 510(k) number is K110487.
When did FLEXIBLE CARDIAC COIL receive FDA 510(k) clearance?
FLEXIBLE CARDIAC COIL received FDA 510(k) clearance on 2011-04-19, under 510(k) number K110487.
Who is the listed applicant for FLEXIBLE CARDIAC COIL?
The FDA 510(k) record lists Lbds Holding Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE CARDIAC COIL?
The FDA product code for FLEXIBLE CARDIAC COIL is MOS.
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: MOS)
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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