Schoelly Imaging, Inc. is one of 15035 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Schoelly Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VS-100 ILLUMINATION AND IMAGING SYSTEM, FSC 2, NASO-LARYNGO-PHARYNGOSCOPE
5
Total
5
Cleared
0
Denied
Schoelly Imaging, Inc. has 5 FDA 510(k) cleared medical devices. Based in Ayer, US.
Historical record: 5 cleared submissions from 2006 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Schoelly Imaging, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Schoelly Imaging, Inc.
5 devices
Cleared
May 18, 2009
VS-100 ILLUMINATION AND IMAGING SYSTEM
Gastroenterology & Urology
55d
Cleared
May 11, 2009
FSC 2
Gastroenterology & Urology
67d
Cleared
Jan 16, 2009
NASO-LARYNGO-PHARYNGOSCOPE
Ear, Nose, Throat
46d
Cleared
Mar 02, 2007
FLEXILUX II CYSTOSCOPE AND HYSTEROSCOPE
Gastroenterology & Urology
333d
Cleared
Feb 23, 2006
FLEXISCOPE, MODELS 50MH AND 50 MHC
General & Plastic Surgery
78d