PREVIEW TREATMENT PLANNING SOFTWARE
K-Number: K040852 · 2004-04-23
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Device Summary
Frequently Asked Questions
What is the PREVIEW TREATMENT PLANNING SOFTWARE?
PREVIEW TREATMENT PLANNING SOFTWARE is a medical device that received FDA 510(k) clearance on 2004-04-23. The listed applicant is Medical Media Systems, Inc.. The 510(k) number is K040852.
When did PREVIEW TREATMENT PLANNING SOFTWARE receive FDA 510(k) clearance?
PREVIEW TREATMENT PLANNING SOFTWARE received FDA 510(k) clearance on 2004-04-23, under 510(k) number K040852.
Who is the listed applicant for PREVIEW TREATMENT PLANNING SOFTWARE?
The FDA 510(k) record lists Medical Media Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREVIEW TREATMENT PLANNING SOFTWARE?
The FDA product code for PREVIEW TREATMENT PLANNING SOFTWARE is LLZ.
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.
Related Devices (Code: LLZ)
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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