510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K942269Substantially Equivalent

Medtronic Everest Inflation Device

Medtronics Interventional Vascular, Danvers MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K942269 is the FDA 510(k) clearance record for MEDTRONIC EVEREST INFLATION DEVICE, a class II device, cleared for Medtronics Interventional Vascular on under FDA product code MAV (Syringe, Balloon Inflation). FDA records list 21 510(k) clearances for Medtronics Interventional Vascular, from to . As of , FDA records show 5 recalls naming K942269.

Clearance record

Decision date
Received
(161 days to decision)
Product code
MAV Syringe, Balloon Inflation
Regulation
21 CFR 870.1650
Device class
Class II
Review panel
Cardiovascular
Applicant
Medtronics Interventional Vascular 37a Cherry Hill Dr., Danvers MA
510(k) summary
Summary
Third party review
No

Clearances, product code MAV

Trailing 12 months
1 clearance under product code MAV in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MAV, 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 20261
October 20260