Interspec, Inc.
Interspec, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1994.
Top product codes for Interspec, Inc.
Recent clearances by Interspec, Inc.
- K940671 — INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND FLOWMETER
- K924231 — INTERSPEC APOGEE CLA
- K915696 — INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE
- K920678 — ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETER
- K911073 — PROBE REFILL KIT
- K910049 — INTERSPEC APOGEE, MODIFICATION
- K903839 — INTERSPEC APOGEE
- K900155 — INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER
- K892944 — INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515
- K890173 — INTERSPEC APOGEE
- K862913 — CARDIOSCAN WITH DOPPLER OPTION
- K863372 — SM-20 CARDIOSCAN DOPPLER OPTION WITH CFM700 PROBES
- K860568 — ULTRASONIC IMAGING SYSTEM (MODIFIED)
- K860579 — CARDIOSCAN DOPPLER OPTION
- K841263 — CARDIOSCAN - TM BEING APPLIED FOR
- K841110 — NEUROTRAC
- K823116 — NEUROTRAC
Data sourced from openFDA. This site is unofficial and independent of the FDA.