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
K780501Substantially Equivalent

Electrode Tester

Mg Medical Electronics, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780501 is the FDA 510(k) clearance record for ELECTRODE TESTER, a class II device, cleared for Mg Medical Electronics on under FDA product code KRC (Tester, Electrode, Surface, Electrocardiographic). FDA records list one 510(k) clearance for Mg Medical Electronics. As of , FDA records show no recalls naming K780501.

Clearance record

Decision date
Received
(52 days to decision)
Product code
KRC Tester, Electrode, Surface, Electrocardiographic
Regulation
21 CFR 870.2370
Device class
Class II
Review panel
Cardiovascular
Applicant
Mg Medical Electronics 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KRC

Trailing 12 months

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

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