510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K980241Substantially Equivalent

Netco Medical Data Transportation Service Software

Netco Communications Corp., Minneapolis MN / Traditional, Substantially Equivalent

K980241 is the FDA 510(k) clearance record for NETCO MEDICAL DATA TRANSPORTATION SERVICE SOFTWARE, a class I device, cleared for Netco Communications Corp. on under FDA product code LMD (System, Digital Image Communications, Radiological). FDA's definition for product code LMD reads: "A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, interfaces, and a communications protocol. It may provide simple...". FDA records list one 510(k) clearance for Netco Communications Corp. As of , FDA records show no recalls naming K980241.

Clearance record

Decision date
Received
(53 days to decision)
Product code
LMD System, Digital Image Communications, Radiological
Regulation
21 CFR 892.2020
Device class
Class I
Review panel
Radiology
Applicant
Netco Communications Corp. 6100 W. 110th St., Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code LMD

Trailing 12 months

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

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