CERACAST-V
K-Number: K030416 · 2003-04-14
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Device Summary
Frequently Asked Questions
What is the CERACAST-V?
CERACAST-V is a medical device that received FDA 510(k) clearance on 2003-04-14. The listed applicant is Mountain Medico, Inc.. The 510(k) number is K030416.
When did CERACAST-V receive FDA 510(k) clearance?
CERACAST-V received FDA 510(k) clearance on 2003-04-14, under 510(k) number K030416.
Who is the listed applicant for CERACAST-V?
The FDA 510(k) record lists Mountain Medico, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERACAST-V?
The FDA product code for CERACAST-V is EJH.
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 Mountain Medico, 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: EJH)
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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