Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K040780Substantially Equivalent

Electrosurgical Pencils

Hangzhou Shuyou Medical Instrument Company, Ltd., West Bloomfield MI / Traditional, Substantially Equivalent

K040780 is the FDA 510(k) clearance record for ELECTROSURGICAL PENCILS, a class II device, cleared for Hangzhou Shuyou Medical Instrument Company, Ltd. on under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list one 510(k) clearance for Hangzhou Shuyou Medical Instrument Company, Ltd. As of , FDA records show no recalls naming K040780.

Clearance record

Decision date
Received
(321 days to decision)
Product code
GEI Electrosurgical, Cutting & Coagulation & Accessories
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Hangzhou Shuyou Medical Instrument Company, Ltd. 6868 Colony Dr., West Bloomfield MI
510(k) summary
Statement
Third party review
No

Clearances, product code GEI

Trailing 12 months
47 clearances under product code GEI in the twelve months to October 2026, June 2026 the highest month at 9.
Show the numbers
Monthly 510(k) clearances under FDA product code GEI, trailing twelve months
MonthClearances
November 20254
December 20251
January 20266
February 20263
March 20265
April 20265
May 20264
June 20269
July 20263
August 20262
September 20265
October 20260