The following data is part of a premarket notification filed by Medical Media Systems, Inc. with the FDA for Preview Treatment Planning Software.
Device ID | K040852 |
510k Number | K040852 |
Device Name: | PREVIEW TREATMENT PLANNING SOFTWARE |
Classification | System, Image Processing, Radiological |
Applicant | MEDICAL MEDIA SYSTEMS, INC. 5610 WISCONSIN AVENUE # 304 Chevy Chase, MD 20815 |
Contact | Patsy J Trisler |
Correspondent | Patsy J Trisler MEDICAL MEDIA SYSTEMS, INC. 5610 WISCONSIN AVENUE # 304 Chevy Chase, MD 20815 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-04-01 |
Decision Date | 2004-04-23 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
B119PREVIEW0 | K040852 | 000 |