PanNAT STEC Test
Jun 2018
221d
Micronics, Inc.
1
Total
1
Cleared
0
Denied
Micronics, Inc. — FDA 510(k) Submissions
Micronics, Inc. has submitted 1 FDA 510(k) premarket notifications since 2018, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Gastrointestinal Bacterial Panel Multiplex Nucleic Acid-based Assay System . Use the specialty filter in the sidebar to narrow results.
1 devices