510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K933050Substantially Equivalent

Changes to Protectiv(tm) & Jelco(tm) Winged Cath

Critikon Company, LLC, Tampa FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933050 is the FDA 510(k) clearance record for CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATH, a class II device, cleared for Critikon Company, LLC on under FDA product code FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days). FDA records list 51 510(k) clearances for Critikon Company, LLC, from to . As of , FDA records show no recalls naming K933050.

Clearance record

Decision date
Received
(208 days to decision)
Product code
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation
21 CFR 880.5200
Device class
Class II
Review panel
General Hospital
Applicant
Critikon Company, LLC 4110 George Rd., Tampa FL
510(k) summary
Summary
Third party review
No

Clearances, product code FOZ

Trailing 12 months
9 clearances under product code FOZ in the twelve months to October 2026, April 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FOZ, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20262
May 20261
June 20260
July 20262
August 20261
September 20261
October 20260