510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K813336Substantially Equivalent

Lazarus-Nelson Peritoneal Lavage Tray

American Pharmaseal Div. Ahsc, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K813336 is the FDA 510(k) clearance record for LAZARUS-NELSON PERITONEAL LAVAGE TRAY, a class II device, cleared for American Pharmaseal Div. Ahsc on under FDA product code FKO (Catheter, Peritoneal Dialysis, Single Use). FDA records list 64 510(k) clearances for American Pharmaseal Div. Ahsc, from to . As of , FDA records show no recalls naming K813336.

Clearance record

Decision date
Received
(24 days to decision)
Product code
FKO Catheter, Peritoneal Dialysis, Single Use
Regulation
21 CFR 876.5630
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
American Pharmaseal Div. Ahsc 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FKO

Trailing 12 months

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

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