510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DWGClass II

Electrosurgical Device

21 CFR 878.4400 / General, Plastic Surgery
FDA source (opens on fda.gov)

DWG is the FDA product code for Electrosurgical Device, a class II device type, regulated under 21 CFR 878.4400. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DWG
Device name
Electrosurgical Device
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code DWG

By decision year
4 clearances under product code DWG with a decision year between 1993 and 1994, 1994 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code DWG by decision year
YearClearances
19931
19943

Applicants with the most clearances

Product code DWG
Applicants holding the most 510(k) clearances under product code DWG
ApplicantClearances
Aspen Labs1
Beacon Laboratories, Inc.1
Conmedcorp1
Mahe Intl., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code