510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K060064Substantially Equivalent

Stethoflux

Odvi, Orsay, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060064 is the FDA 510(k) clearance record for STETHOFLUX, a class II device, cleared for Odvi on under FDA product code JAF (Monitor, Ultrasonic, Nonfetal). FDA records list one 510(k) clearance for Odvi. As of , FDA records show no recalls naming K060064.

Clearance record

Decision date
Received
(91 days to decision)
Product code
JAF Monitor, Ultrasonic, Nonfetal
Regulation
21 CFR 892.1540
Device class
Class II
Review panel
Radiology
Applicant
Odvi 69 Rue De Paris, Orsay, FR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JAF

Trailing 12 months

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

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