Valleylab, Inc. - FDA 510(k) Cleared Devices
94
Total
93
Cleared
0
Denied
Valleylab, Inc. has 93 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 93 cleared submissions from 1976 to 2003.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
94 devices
Cleared
May 29, 2003
LIGASURE 5MM LAPAROSCOPIC SEALER-DIVIDER, MODEL LS1500
General & Plastic Surgery
59d
Cleared
Apr 02, 2001
VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 &...
General & Plastic Surgery
90d
Cleared
Mar 26, 2001
LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100
General & Plastic Surgery
83d
Cleared
Mar 07, 2000
E7512 PREMIE REM POLYHESIVE II PATIENT RETURN ELECTRODE
General & Plastic Surgery
68d
Cleared
Jan 21, 1999
BISURE LAPAROSCOPIC BIPOLAR FORCEPS
General & Plastic Surgery
90d
Cleared
Aug 28, 1998
LIGASURE VESSEL SEALING SYSTEM
General & Plastic Surgery
88d
Cleared
Jul 06, 1998
CUSA EXCEL ULTRASONIC SURGICAL ASPIRATOR SYSTEM
General & Plastic Surgery
90d
Cleared
Jun 29, 1998
VALLEYLAB OPTIMUMM SMOKE EVACUATOR SYSTEM
General Hospital
110d
Cleared
Mar 28, 1997
E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH
General & Plastic Surgery
72d
Cleared
Mar 11, 1997
FORCE ARGON II ARGON ENHANCED ELECTROSURGICAL SYSTEM
General & Plastic Surgery
112d
Cleared
Jan 16, 1997
CUSA SYSTEM 200C ULTRASONIC ASPIRATOR/CUSA SYSTEM 200T ULTRASONIC...
General & Plastic Surgery
59d
Cleared
Jan 09, 1997
DAVIS BAYONET ELECTRODES
General & Plastic Surgery
52d
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