Medical Device Manufacturer · US , Temecula , CA

Merck Millipore , Ltd.

2 submissions · 2 cleared · Since 2014
2
Total
2
Cleared
0
Denied

Merck Millipore , Ltd. — FDA 510(k) Submissions

Merck Millipore , Ltd. has submitted 2 FDA 510(k) premarket notifications since 2014, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filter, Conduction, Anesthetic, Filter, Infusion Line . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 General Hospital 1 Anesthesiology 1