Richard Wolf Medical Instruments Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Richard Wolf Medical Instruments Corp. - FDA 510(k) Cleared Devices
Recent clearances: core nova Complete Operating Room Endoscopy, THE RICHARD WOLF ENDOCAM LOGIC HD CAMERA SYSTEM 5525, ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2
Richard Wolf Medical Instruments Corp. has 142 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 142 cleared submissions from 1977 to 2016.
Browse the FDA 510(k) cleared devices submitted by Richard Wolf Medical Instruments Corp. 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 - Richard Wolf Medical Instruments Corp.
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