FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

The Oligio

K Number: K221989 · Decision Oct 13, 2022
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
28
Review Days
99

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
The Oligio
K Number
K221989
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
Wontech Co., Ltd.
Date Received
July 6, 2022
Decision Date
October 13, 2022
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 Wontech Co., Ltd.

K Number Device Name
K252877 SANDRO Dual
K250165 Pastelle
K251288 Veincare
K251094 Alma Veil
K243957 PICOALEX
K241643 WONTECH Surgical Optic Fibers (BA400/BA400R/BA600/BA600R)
K241527 Pastelle Pro
K243929 Oligio X
K241930 Veincare
K241406 Lavieen
Search all 28 clearances from Wontech Co., Ltd. →