510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023233Substantially Equivalent

Ebi Targetcath Fluoro-Guided Steerable Catheter System

Ebi, LLC, Parsippany NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023233 is the FDA 510(k) clearance record for EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM, a class II device, cleared for Ebi, L.P. on under FDA product code BSO (Catheter, Conduction, Anesthetic). FDA records list 99 510(k) clearances for Ebi, L.P., from to . As of , FDA records show one recall naming K023233.

Clearance record

Decision date
Received
(77 days to decision)
Product code
BSO Catheter, Conduction, Anesthetic
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Applicant
Ebi, L.P. 399 Jefferson Rd., Parsippany NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BSO

Trailing 12 months

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

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