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

LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100

K Number: K010013 · Decision Mar 26, 2001
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
94
Review Days
83

Basic Information

Device Name
LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100
K Number
K010013
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
March 26, 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

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