510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K210394Substantially Equivalent

Electrosurgical accessory

Dornier Medtech America, Inc., Kennesaw GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210394 is the FDA 510(k) clearance record for Electrosurgical accessory, a class II device, cleared for Dornier Medtech America, Inc. on under FDA product code FAS (Electrode, Electrosurgical, Active, Urological). FDA records list 46 510(k) clearances for Dornier Medtech America, Inc., from to . As of , FDA records show no recalls naming K210394.

Clearance record

Decision date
Received
(98 days to decision)
Product code
FAS Electrode, Electrosurgical, Active, Urological
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Dornier Medtech America, Inc. 1155 Roberts Blvd., Suite 100, Kennesaw GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FAS

Trailing 12 months
1 clearance under product code FAS in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FAS, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260