Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K832012Substantially Equivalent

Medical Electronics-Printer Clock

Litton Medical Electronics, Mchenry IL / Traditional, Substantially Equivalent

K832012 is the FDA 510(k) clearance record for MEDICAL ELECTRONICS-PRINTER CLOCK, a class I device, cleared for Litton Medical Electronics on under FDA product code DSF (Recorder, Paper Chart). FDA records list 38 510(k) clearances for Litton Medical Electronics, from to . As of , FDA records show no recalls naming K832012.

Clearance record

Decision date
Received
(130 days to decision)
Product code
DSF Recorder, Paper Chart
Regulation
21 CFR 870.2810
Device class
Class I
Review panel
Cardiovascular
Applicant
Litton Medical Electronics 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DSF

Trailing 12 months

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

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