RTDOSEPLAN
K-Number: K022961 · 2003-01-31
Advertisement
Device Summary
Frequently Asked Questions
What is the RTDOSEPLAN?
RTDOSEPLAN is a medical device that received FDA 510(k) clearance on 2003-01-31. The listed applicant is Math Resolutions, LLC. The 510(k) number is K022961.
When did RTDOSEPLAN receive FDA 510(k) clearance?
RTDOSEPLAN received FDA 510(k) clearance on 2003-01-31, under 510(k) number K022961.
Who is the listed applicant for RTDOSEPLAN?
The FDA 510(k) record lists Math Resolutions, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RTDOSEPLAN?
The FDA product code for RTDOSEPLAN 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 Math Resolutions, LLC 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.
Advertisement