510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K881478Substantially Equivalent

Modified Keymed Flexible Esophageal Dilators

KEYMED (Medical & Industrial Equipment) Ltd, Essex, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K881478 is the FDA 510(k) clearance record for MODIFIED KEYMED FLEXIBLE ESOPHAGEAL DILATORS, a class II device, cleared for Keymed (Medical & Industrial Equipment), Ltd. on under FDA product code KNQ (Dilator, Esophageal). FDA records list 7 510(k) clearances for Keymed (Medical & Industrial Equipment), Ltd., from to . As of , FDA records show no recalls naming K881478.

Clearance record

Decision date
Received
(161 days to decision)
Product code
KNQ Dilator, Esophageal
Regulation
21 CFR 876.5365
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Keymed (Medical & Industrial Equipment), Ltd. Keymed House,Stock Rd., Essex, GB
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