DWG — Electrosurgical Device Class II

FDA Device Classification

FDA product code DWG covers "Electrosurgical Device", a Class II medical device regulated under 21 CFR 878.4400. Submissions are reviewed by the General, Plastic Surgery panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
DWG
Device Class
Class II
Regulation Number
878.4400
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K942823mahe intlMAHE INSTRUMENTSDecember 5, 1994
K932345conmedcorpTECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USEApril 12, 1994
K931215aspen labsHAND-TROL SMarch 28, 1994
K925708beacon laboratoriesDISPOSABLE ELECTROSURGERY BALL ELECTRODEApril 20, 1993