510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001498Substantially Equivalent

The Fugo Blade

Medisurg, Ltd., Norristown PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001498 is the FDA 510(k) clearance record for THE FUGO BLADE, a class II device, cleared for Medisurg , Ltd. on under FDA product code NCR (Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered). FDA records list 4 510(k) clearances for Medisurg , Ltd., from to . As of , FDA records show one recall naming K001498.

Clearance record

Decision date
Received
(87 days to decision)
Product code
NCR Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered
Regulation
21 CFR 886.4100
Device class
Class II
Review panel
Ophthalmic
Applicant
Medisurg , Ltd. 100 W. Fornance St., Norristown PA
510(k) summary
Statement
Third party review
No

Clearances, product code NCR

Trailing 12 months

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

FDA records show no clearances under product code NCR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NCR, 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