510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K103668Substantially Equivalent

Bnx Fine Needle Aspiration System

Boston Endoscopic Engineering, Foster RI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K103668 is the FDA 510(k) clearance record for BNX FINE NEEDLE ASPIRATION SYSTEM, a class II device, cleared for Boston Endoscopic Engineering on under FDA product code FCG (Biopsy Needle). FDA records list one 510(k) clearance for Boston Endoscopic Engineering. As of , FDA records show 5 recalls naming K103668.

Clearance record

Decision date
Received
(14 days to decision)
Product code
FCG Biopsy Needle
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Boston Endoscopic Engineering 53 Kennedy Rd., Foster RI
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code FCG

Trailing 12 months

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

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