Microworld Medical Instruments, Inc. is one of 24559 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microworld Medical Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: COLIBRI DISPOSABLE VITRECTOMY CUTTER
1
Total
1
Cleared
0
Denied
Microworld Medical Instruments, Inc. has 1 FDA 510(k) cleared medical devices. Based in Oakland, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Microworld Medical Instruments, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Microworld Medical Instruments, Inc.
1 devices