FDA 510(k) Applications Submitted by Samuel Wade

FDA 510(k) Number Submission Date Device Name Applicant
K183199 11/19/2018 TRIO Handpiece OmniGuide, Inc.
K023543 10/22/2002 EVLT KIT AND D15PLUS AND D30PLUS DIODE DIOMED, INC.
K974300 11/17/1997 TELEMED SYSTEMS RETRIEVAL BASKET TELEMED SYSTEMS, INC.
K974312 11/17/1997 REUSABLE BIOPSY FORCEPS OVAL CUP, REUSABLE BIOSY FORCEPS OVAL CUP W/NEEDLE, REUSABLE BIOPSY FORCEPS SERRATED CUP, REUSAR TELEMED SYSTEMS, INC.


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