Device Classification Name |
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device |
510(K) Number |
K221277 |
Device Name |
Electrosurgical, Cutting & Coagulation & Accessories |
Applicant |
RF Medical Co., Ltd
#502, 503, 506, 511, 254, Beotkkot-ro, Geumcheon-gu,
Seoul 08511 KR
Other 510(k) Applications for this Company
|
Contact |
Kwang S Choi
Other 510(k) Applications for this Contact |
Regulation Number |
878.4400
More FDA Info for this Regulation Number |
Classification Product Code |
GEI
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
05/03/2022 |
Decision Date |
09/02/2022 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
SU - General & Plastic Surgery |
Review Advisory Committee |
SU - General & Plastic Surgery |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|