Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM

K-Number: K992753 · 1999-09-03

Decision Date1999-09-03
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K992753. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM?

CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K992753.

When did CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM receive FDA 510(k) clearance?

CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM received FDA 510(k) clearance on 1999-09-03, under 510(k) number K992753.

Who is the listed applicant for CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM?

The FDA product code for CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM 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 Varian Assoc., 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.

View all 86 devices →

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.

↑