Medical Device Manufacturer · US , Mchenry , IL

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

17 submissions · 16 cleared · Since 1982

17

Total

16

Cleared

0

Denied

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

7 devices

1-7 of 7

Cleared Apr 29, 1991

INTERSPEC APOGEE, MODIFICATION

Cardiovascular · 112d

Cleared Nov 16, 1990

INTERSPEC APOGEE

Cardiovascular · 87d

Cleared Jul 19, 1989

INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515

Cardiovascular · 89d

Cleared Nov 04, 1986

CARDIOSCAN WITH DOPPLER OPTION

Cardiovascular · 95d

Cleared Nov 04, 1986

SM-20 CARDIOSCAN DOPPLER OPTION WITH CFM700 PROBES

Cardiovascular · 63d

Cleared Jun 30, 1986

CARDIOSCAN DOPPLER OPTION

Cardiovascular · 132d

Cleared Oct 19, 1984

CARDIOSCAN - TM BEING APPLIED FOR

Cardiovascular · 207d