510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K812685Substantially Equivalent

Ericka Neg. Pressure Arterial Blood Line

Ericka, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812685 is the FDA 510(k) clearance record for ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE, a class II device, cleared for Ericka on under FDA product code FJK (Set, Tubing, Blood, With And Without Anti-Regurgitation Valve). FDA records list one 510(k) clearance for Ericka. As of , FDA records show no recalls naming K812685.

Clearance record

Decision date
Received
(7 days to decision)
Product code
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Ericka 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FJK

Trailing 12 months
2 clearances under product code FJK in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FJK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260