Medical Device Manufacturer · US , Mchenry , IL

Interspec, Inc. - FDA 510(k) Cleared Devices

17 submissions · 16 cleared · Since 1982

Total

Cleared

Denied

Interspec, Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 16 cleared submissions from 1982 to 1994. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Interspec, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Interspec, Inc.

17 devices

1-12 of 17

Cleared Nov 22, 1994

INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND...

INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE

K915696 · ITX

Radiology · 337d

Cleared Apr 02, 1992

ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETER

INTERSPEC APOGEE, MODIFICATION

K910049 · DPW

Cardiovascular · 112d

INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER

K900155 · ITX

Radiology · 266d

Cleared Jul 19, 1989

INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515

CARDIOSCAN WITH DOPPLER OPTION

K862913 · JOP

Cardiovascular · 95d

Cleared Nov 04, 1986

SM-20 CARDIOSCAN DOPPLER OPTION WITH CFM700 PROBES

K863372 · DPT

Cardiovascular · 63d

Interspec, Inc. - FDA 510(k) Cleared Devices

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