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
K020780Substantially Equivalent

Transtar Intracranial Pressure Transducer, Model Mx950icp

Medex, Inc., Dublin OH / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K020780 is the FDA 510(k) clearance record for TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP, a class II device, cleared for Medex, Inc. on under FDA product code GWM (Device, Monitoring, Intracranial Pressure). FDA records list 12 510(k) clearances for Medex, Inc., from to . As of , FDA records show 2 recalls naming K020780.

Clearance record

Decision date
Received
(70 days to decision)
Product code
GWM Device, Monitoring, Intracranial Pressure
Regulation
21 CFR 882.1620
Device class
Class II
Review panel
Neurology
Applicant
Medex, Inc. 6250 Shier Rings Rd., Dublin OH
510(k) summary
Statement
Third party review
No

Clearances, product code GWM

Trailing 12 months
1 clearance under product code GWM in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GWM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260