FDA 510(k) Applications Submitted by ARTHUR SCHENCK

FDA 510(k) Number Submission Date Device Name Applicant
K892944 04/21/1989 INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515 INTERSPEC, INC.
K915696 12/23/1991 INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE INTERSPEC, INC.
K910049 01/07/1991 INTERSPEC APOGEE, MODIFICATION INTERSPEC, INC.
K900155 01/12/1990 INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER INTERSPEC, INC.
K940671 02/16/1994 INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND FLOWMETER INTERSPEC, INC.
K911073 03/11/1991 PROBE REFILL KIT INTERSPEC, INC.
K924231 08/21/1992 INTERSPEC APOGEE CLA INTERSPEC, INC.


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