510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K990935Substantially Equivalent

Jackson Esophageal Dilator

Pilling Weck Surgical, Fort Washington PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K990935 is the FDA 510(k) clearance record for JACKSON ESOPHAGEAL DILATOR, a class II device, cleared for Pilling Weck Surgical on under FDA product code KNQ (Dilator, Esophageal). FDA records list 5 510(k) clearances for Pilling Weck Surgical, from to . As of , FDA records show no recalls naming K990935.

Clearance record

Decision date
Received
(59 days to decision)
Product code
KNQ Dilator, Esophageal
Regulation
21 CFR 876.5365
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Pilling Weck Surgical 420 Delaware Dr., Fort Washington PA
510(k) summary
Summary
Third party review
No

Clearances, product code KNQ

Trailing 12 months

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

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