DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS
K-Number: K051799 · 2005-11-02
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS?
DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS is a medical device that received FDA 510(k) clearance on 2005-11-02. The listed applicant is Coeur, Inc.. The 510(k) number is K051799.
When did DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS receive FDA 510(k) clearance?
DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS received FDA 510(k) clearance on 2005-11-02, under 510(k) number K051799.
Who is the listed applicant for DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS?
The FDA 510(k) record lists Coeur, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS?
The FDA product code for DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS is DXT.
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 Coeur, 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: DXT)
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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