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
K072766Substantially Equivalent

Pvmed Ddr 2520 Digital Imaging System

Portavision Medical, LLC, Austin TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072766 is the FDA 510(k) clearance record for PVMED DDR 2520 DIGITAL IMAGING SYSTEM, a class II device, cleared for Portavision Medical on under FDA product code IXK (System, Imaging, X-Ray, Electrostatic). FDA records list 6 510(k) clearances for Portavision Medical, from to . As of , FDA records show no recalls naming K072766.

Clearance record

Decision date
Received
(74 days to decision)
Product code
IXK System, Imaging, X-Ray, Electrostatic
Regulation
21 CFR 892.1630
Device class
Class II
Review panel
Radiology
Applicant
Portavision Medical 1705 S. Capital Of Texas Hwy.,, Austin TX
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code IXK

Trailing 12 months

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

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