ICAD SYSTEM

Analyzer, Medical Image

FDA Premarket Approval P010038 S007

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 replacing the icad system's cad software with the second look cad software and increasing the system memory from 1 gigabyte to 2 gigabytes. The device, as modified, will be marketed under the trade name second look 200 and is indicated for: second look is a computed system intended to identify and mark regions of interest on standard mammographic views, including views from patients with breast implants and images from qualified full field digital mammography systems, to bring to the attention of the radiologist after the initial reading has been completed. Thus, the system assists the radiologist in minimizing observational oversights by identifying areas on the original mammogram that may warrant a second review.

DeviceICAD SYSTEM
Classification NameAnalyzer, Medical Image
Generic NameAnalyzer, Medical Image
ApplicantICAD, INC.
Date Received2004-04-28
Decision Date2004-05-19
PMAP010038
SupplementS007
Product CodeMYN
Advisory CommitteeRadiology
Supplement TypeReal-time Process
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address ICAD, INC. 98 Spit Brook Road suite 100 nashua, NH 03062

Supplemental Filings

Supplement NumberDateSupplement Type
P010038Original Filing
S017 2012-10-05 Normal 180 Day Track
S016 2012-08-10 Normal 180 Day Track
S015 2008-05-19 Normal 180 Day Track No User Fee
S014 2007-04-02 Normal 180 Day Track No User Fee
S013 2006-12-18 Normal 180 Day Track
S012 2006-07-12 Normal 180 Day Track
S011
S010 2005-10-18 Normal 180 Day Track No User Fee
S009 2005-01-18 Normal 180 Day Track No User Fee
S008 2004-06-24 Normal 180 Day Track
S007 2004-04-28 Real-time Process
S006 2004-04-26 Normal 180 Day Track No User Fee
S005 2003-07-29 Normal 180 Day Track
S004 2003-06-18 Normal 180 Day Track
S003 2003-02-10 Normal 180 Day Track
S002 2002-10-28 Real-time Process
S001 2002-10-28 Normal 180 Day Track

NIH GUDID Devices

Device IDPMASupp
00858012005007 P010038 012
00858012005830 P010038 013
00858012005823 P010038 013
00858012005809 P010038 013
00858012005175 P010038 013
00858012005168 P010038 013
00858012005151 P010038 013
00858012005144 P010038 013
00858012005137 P010038 013
00858012005120 P010038 013
00858012005113 P010038 013
00858012005106 P010038 013
00858012005847 P010038 013
00858012005861 P010038 013
00858012005014 P010038 013
00858012005854 P010038 013
00858012005816 P010038 013
00858012005793 P010038 013
00858012005601 P010038 013
00858012005083 P010038 013
00858012005076 P010038 013
00858012005052 P010038 013
00858012005038 P010038 013
00858012005021 P010038 013
00858012005090 P010038 013
00858012005069 P010038 016
00858012005045 P010038 017

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.