Medical Device Manufacturer · US , Portland , OR

Virtual Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1985

Total

Cleared

Denied

Virtual Corp. has 9 FDA 510(k) cleared medical devices. Based in Portland, US.

Historical record: 9 cleared submissions from 1985 to 1996. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Virtual Corp. Filter by specialty or product code using the sidebar.

Virtual Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Virtual Corp.

9 devices

1-9 of 9

Cleared Apr 03, 1996

THE VIRTUAL M-332

K960500 · EWD

Ear, Nose, Throat · 61d

Cleared May 10, 1994

MODEL 222 CLINICAL AUDIOMETER

K934715 · EWO

Ear, Nose, Throat · 221d

Cleared Jul 08, 1993

MODEL 322 CLINICAL AUDIOMETER

K930203 · EWD

Ear, Nose, Throat · 175d

Cleared Mar 29, 1993

MODEL 330 SCREENING AUDIO METER, MODIFIED

K926574 · GWJ

Neurology · 89d

Cleared Oct 21, 1991

MODEL 330 SCREENING AUDIOMETER

K911689 · EWO

Ear, Nose, Throat · 188d

Cleared Jan 16, 1990

MODEL 210 IMPEDANCE SYSTEM

K895443 · ETY

Ear, Nose, Throat · 130d

Cleared Jan 16, 1990

MODEL 340 PROBE MIC SYSTEM

K896301 · ETW

Ear, Nose, Throat · 78d

Cleared Nov 18, 1986

MODEL 320 TWO CHANNEL AUDIOMETER

K863984 · EWO

Ear, Nose, Throat · 35d

Cleared Dec 18, 1985

MODEL 310 IMPEDANCE SYSTEM

K853863 · ETY

Ear, Nose, Throat · 92d

Virtual Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Virtual Corp.

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