510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993149Substantially Equivalent

Peritoneal Dialysis Catheters and Adapters

Medionics International, Inc., Markham, Ontario, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K993149 is the FDA 510(k) clearance record for PERITONEAL DIALYSIS CATHETERS AND ADAPTERS, a class II device, cleared for Medionics International, Inc. on under FDA product code FJS (Catheter, Peritoneal, Long-Term Indwelling). FDA records list 10 510(k) clearances for Medionics International, Inc., from to . As of , FDA records show no recalls naming K993149.

Clearance record

Decision date
Received
(220 days to decision)
Product code
FJS Catheter, Peritoneal, Long-Term Indwelling
Regulation
21 CFR 876.5630
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medionics International, Inc. 114 Anderson Ave., Markham, Ontario, CA
510(k) summary
Statement
Third party review
No

Clearances, product code FJS

Trailing 12 months

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

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