Medical Device Manufacturer · US , Littleton , MA

Doran Instruments, Inc.

2 submissions · 2 cleared · Since 1986

Total

Cleared

Denied

Doran Instruments, Inc. — FDA 510(k) Submissions

Doran Instruments, Inc. has submitted 2 FDA 510(k) premarket notifications since 1986, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Photic, Evoked Response, Electrode, Corneal . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

GOLDLENS(TM)

K913239 · HLZ Electrode, Corneal · Ophthalmic

Jan 1992 193d

MACULOSCOPE(TM)

K863956 · GWE Stimulator, Photic,... · Neurology

Nov 1986 34d

Data Source

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

Doran Instruments, Inc.

Doran Instruments, Inc. — FDA 510(k) Submissions

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