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

LIGER MEDICAL ESU-110

K Number: K133273 · Decision Feb 12, 2014
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
3
Review Days
111

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LIGER MEDICAL ESU-110
K Number
K133273
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
Liger Medical, LLC
Date Received
October 24, 2013
Decision Date
February 12, 2014
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 Liger Medical, LLC

K Number Device Name
K202915 IRIS Thermocoagulator and Digital Colposcope
K152843 Liger Medical HTU-110