Appasamy Associates is one of 168 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Appasamy Associates - FDA 510(k) Cleared Devices
Recent clearances: AAIO-7, AAIO WIRLESS, APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIES
2
Total
2
Cleared
0
Denied
Appasamy Associates has 2 FDA 510(k) cleared medical devices. Based in Arumbakkam, Chennai, IN.
Historical record: 2 cleared submissions from 2008 to 2011. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Appasamy Associates 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 - Appasamy Associates
2 devices