510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781678Substantially Equivalent

Defibrillator, Mark II

Ipco Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781678 is the FDA 510(k) clearance record for DEFIBRILLATOR, MARK II, a class II device, cleared for Ipco Corp. on under FDA product code LDD (Dc-Defibrillator, Low-Energy, (Including Paddles)). FDA records list 13 510(k) clearances for Ipco Corp., from to . As of , FDA records show no recalls naming K781678.

Clearance record

Decision date
Received
(71 days to decision)
Product code
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
Regulation
21 CFR 870.5300
Device class
Class II
Review panel
Cardiovascular
Applicant
Ipco Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LDD

Trailing 12 months

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

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