FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 & SLIGAURE GENERATOR

K Number: K010010 · Decision Apr 2, 2001
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
94
Review Days
90

Basic Information

Device Name
VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 & SLIGAURE GENERATOR
K Number
K010010
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VALLEYLAB, INC.
Date Received
January 2, 2001
Decision Date
April 2, 2001
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), ordered by most recent decision date.

View all

Other Clearances by VALLEYLAB, INC.

K Number Device Name
K031011 LIGASURE 5MM LAPAROSCOPIC SEALER-DIVIDER, MODEL LS1500
K010013 LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100
K994428 E7512 PREMIE REM POLYHESIVE II PATIENT RETURN ELECTRODE
K983743 BISURE LAPAROSCOPIC BIPOLAR FORCEPS
K981916 LIGASURE VESSEL SEALING SYSTEM
K981262 CUSA EXCEL ULTRASONIC SURGICAL ASPIRATOR SYSTEM
K980915 VALLEYLAB OPTIMUMM SMOKE EVACUATOR SYSTEM
K970140 E0520-TRIGGER SWITCH AND CORD/E0521-TRIGGER SWITCH
K964636 FORCE ARGON II ARGON ENHANCED ELECTROSURGICAL SYSTEM
K964601 CUSA SYSTEM 200C ULTRASONIC ASPIRATOR/CUSA SYSTEM 200T ULTRASONIC ASPIRATOR/CUSA LAP ACCESSORY
Search all 94 clearances from VALLEYLAB, INC. →