Medical Device Manufacturer · US , San Leandro , CA

Parameter Developments, Inc.

1 submissions · 1 cleared · Since 1998
1
Total
1
Cleared
0
Denied

Parameter Developments, Inc. — FDA 510(k) Submissions

Parameter Developments, Inc. has submitted 1 FDA 510(k) premarket notifications since 1998, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Digital Image Storage, Radiological . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Radiology 1