510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K993306Substantially Equivalent

Nikopad Electrosurgical Grounding Pad (*or Sold Under Commercial Names), Model 4760 (Typically)

Paladin Medical, Inc., Stillwater MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K993306 is the FDA 510(k) clearance record for NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY), a class II device, cleared for Paladin Medical, Inc. on under FDA product code HAM (Apparatus, Electrosurgical). FDA records list 14 510(k) clearances for Paladin Medical, Inc., from to . As of , FDA records show no recalls naming K993306.

Clearance record

Decision date
Received
(30 days to decision)
Product code
HAM Apparatus, Electrosurgical
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Paladin Medical, Inc. P.O. Box 560, Stillwater MN
510(k) summary
Summary
Third party review
No

Clearances, product code HAM

Trailing 12 months

FDA records hold no clearances under product code HAM in the trailing twelve months.

FDA records show no clearances under product code HAM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HAM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260