Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K913811Substantially Equivalent

Fukuda Denshi Model Fcp-4101

Fukuda Denshi USA, Inc., Redmond WA / Traditional, Substantially Equivalent

K913811 is the FDA 510(k) clearance record for FUKUDA DENSHI MODEL FCP-4101, cleared for Fukuda Denshi USA, Inc. on under FDA product code LOS. FDA records list 68 510(k) clearances for Fukuda Denshi USA, Inc., from to . As of , FDA records show no recalls naming K913811.

Clearance record

Decision date
Received
(105 days to decision)
Product code
LOS
Review panel
Unknown
Applicant
Fukuda Denshi USA, Inc. 7102-A 180th Ave. Northeast, Redmond WA
510(k) summary
Statement
Third party review
No

Clearances, product code LOS

Trailing 12 months

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

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