510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902124Substantially Equivalent

Dowd Catheter

Boston Scientific Corporation, Watertown MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902124 is the FDA 510(k) clearance record for DOWD CATHETER, a class II device, cleared for Boston Scientific Corp on under FDA product code FAH (Dilator, Urethral, Mechanical). FDA records list 1,110 510(k) clearances for Boston Scientific Corp, from to . As of , FDA records show no recalls naming K902124.

Clearance record

Decision date
Received
(90 days to decision)
Product code
FAH Dilator, Urethral, Mechanical
Regulation
21 CFR 876.5520
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Boston Scientific Corp 480 Pleasant St., Watertown MA
Third party review
No

Clearances, product code FAH

Trailing 12 months

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

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