Medical Device Manufacturer · US , Menlo Park , CA

Iscience Interventional

1 submissions · 1 cleared · Since 2008

Total

Cleared

Denied

Iscience Interventional — FDA 510(k) Submissions

Iscience Interventional has submitted 1 FDA 510(k) premarket notifications since 2008, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoilluminator . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

ISCIENCE INTERVENTIONAL OPHTHALMIC MICROCATHETER

K080067 · MPA Endoilluminator · Ophthalmic

Jul 2008 190d

Iscience Interventional

Iscience Interventional — FDA 510(k) Submissions

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