Fischer Industries, Inc. is one of 25823 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fischer Industries, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LEVEL 356 X-RAY FILM PROCESSOR, MODELS MD & MD-D, X-RAY FILM PROCESSOR, FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND
3
Total
3
Cleared
0
Denied
Fischer Industries, Inc. has 3 FDA 510(k) cleared medical devices. Based in Geneva, US.
Historical record: 3 cleared submissions from 1986 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Fischer Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fischer Industries, Inc.
3 devices