Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K951732Substantially Equivalent

Nezhat-Doresey Pencil-Grip Handles

American Hydro-Surgical Instruments, Inc., Delray Beach FL / Traditional, Substantially Equivalent

K951732 is the FDA 510(k) clearance record for NEZHAT-DORESEY PENCIL-GRIP HANDLES, a class II device, cleared for American Hydro-Surgical Instruments, Inc. 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 18 510(k) clearances for American Hydro-Surgical Instruments, Inc., from to . As of , FDA records show no recalls naming K951732.

Clearance record

Decision date
Received
(40 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
American Hydro-Surgical Instruments, Inc. 430 Commerce Dr., Delray Beach FL
510(k) summary
Summary
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