Pacific Instruments - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pacific Instruments has 1 FDA 510(k) cleared medical devices. Based in Honolulu, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pacific Instruments Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Novare Medical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pacific Instruments
1 devices