NOMOS CORVUS 5.0M
K-Number: K032209 · 2003-08-21
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Device Summary
Frequently Asked Questions
What is the NOMOS CORVUS 5.0M?
NOMOS CORVUS 5.0M is a medical device that received FDA 510(k) clearance on 2003-08-21. The listed applicant is Nomos Corp.. The 510(k) number is K032209.
When did NOMOS CORVUS 5.0M receive FDA 510(k) clearance?
NOMOS CORVUS 5.0M received FDA 510(k) clearance on 2003-08-21, under 510(k) number K032209.
Who is the listed applicant for NOMOS CORVUS 5.0M?
The FDA 510(k) record lists Nomos Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOMOS CORVUS 5.0M?
The FDA product code for NOMOS CORVUS 5.0M is MUJ.
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 Nomos 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: MUJ)
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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