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FDA 510(k)

PREVIEW TREATMENT PLANNING SOFTWARE

K-Number: K040852 · 2004-04-23

Decision Date2004-04-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PREVIEW TREATMENT PLANNING SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Media Systems, Inc.. It received FDA 510(k) clearance on 2004-04-23 under 510(k) number K040852. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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