Medical Device Manufacturer · US , Monument , CO

Prescott'S, Inc.

2 submissions · 2 cleared · Since 1989

Total

Cleared

Denied

Prescott'S, Inc. — FDA 510(k) Submissions

Prescott'S, Inc. has submitted 2 FDA 510(k) premarket notifications since 1989, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Microscope, Operating & Accessories, Ac-powered, Ophthalmic, Sponge, Ophthalmic . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

PRESCOTT'S SURGICAL SPEAR

K003842 · HOZ Sponge, Ophthalmic · Ophthalmic

Apr 2001 122d

MICROSCOPE KNOB COVER, STERILE, DISPOSABLE

K891001 · HRM Microscope, Operating &... · General & Plastic Surgery

Apr 1989 43d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Prescott'S, Inc.

Prescott'S, Inc. — FDA 510(k) Submissions

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