Haas Software is one of 24577 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Haas Software has 1 FDA 510(k) cleared medical devices. Based in Mill Valley, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Haas Software Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Haas Software
1 devices