KODAK DIRECTVIEW CR MAMMOGRAPHY FEATURE

FDA Premarket Approval P080018 S001

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval for the kodak directview cr mammography system. The kodak directview cr mammography feature together with kodak directview cr mammography cassette comprise a device which when used in conjunction with a kodak directview cr system and a mammographic x-ray machine, generates digital mammographic images that can be used for screening and diagnosis of breast cancer. It is intended for use in the same clinical applications as traditional screen-film based mammographic systems. The mammographic images can be interpreted by a qualified physician using either hard copy film or soft copy display at a workstation.

DeviceKODAK DIRECTVIEW CR MAMMOGRAPHY FEATURE
Generic NameFull Field Digital, System, X-ray, Mammographic
ApplicantCARESTREAM HEALTH, INC.
Date Received2010-11-03
Decision Date2010-12-01
PMAP080018
SupplementS001
Product CodeMUE 
Advisory CommitteeRadiology
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address CARESTREAM HEALTH, INC. 150 Verona Street rochester, NY 14608

Supplemental Filings

Supplement NumberDateSupplement Type
P080018Original Filing
S001 2010-11-03 Normal 180 Day Track

NIH GUDID Devices

Device IDPMASupp
60889978869848 P080018 000
60889971290380 P080018 000
60889971342867 P080018 000
60889971508270 P080018 000
60889971667571 P080018 000
60889971790316 P080018 000
60889978156184 P080018 000
60889978188345 P080018 000
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60889971650511 P080018 000
60889971717443 P080018 000
60889978346134 P080018 000
60889978359158 P080018 000
60889978364763 P080018 000
60889978463329 P080018 000
60889978611614 P080018 000
60889971044297 P080018 000

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