Green OR Reprocessed Aquamantys Bipolar Sealer
Apr 2022
350d
Green Or, LLC
1
Total
1
Cleared
0
Denied
Green Or, LLC — FDA 510(k) Submissions
Green Or, LLC has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed . Use the specialty filter in the sidebar to narrow results.
1 devices