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FDA 510(k) Applications Submitted by SAM WADE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140122
01/16/2014
CANDELA GENTLEMAX FAMILY OF LASER SYSTEM
CANDELA CORP.
K120510
02/21/2012
TRANSCEND
SYNERON MEDICAL LTD.
K140732
03/24/2014
CANDELA GENTLELASE FAMILY OF LASER SYSTEMS
CANDELA CORP.
K180993
04/16/2018
Beacon Advanced CO2 Laser System
OmniGuide, Inc
K122579
08/23/2012
VELASHAPE
SYNERON MEDICAL LTD.
K112715
09/19/2011
CANDELA GENTLEMAX FAMILY OF LASERS
CANDELA CORP.
K133283
10/25/2013
CANDELA GENTLEMAX FAMILY OF LASER SYSTEMS
CANDELA CORP.
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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