510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900583Substantially Equivalent

Modified Bivona Epistaxis Catheter

Bivona Medical Technologies, Gary IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900583 is the FDA 510(k) clearance record for MODIFIED BIVONA EPISTAXIS CATHETER, a class I device, cleared for Bivona Medical Technologies on under FDA product code EMX (Balloon, Epistaxis). FDA records list 50 510(k) clearances for Bivona Medical Technologies, from to . As of , FDA records show no recalls naming K900583.

Clearance record

Decision date
Received
(183 days to decision)
Product code
EMX Balloon, Epistaxis
Regulation
21 CFR 874.4100
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Bivona Medical Technologies 5700 W. 23rd Ave., Gary IN
Third party review
No

Clearances, product code EMX

Trailing 12 months

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

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