510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800936Substantially Equivalent

R2 Paddle Type Cable-Adaptor #S 170,171

R2 Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800936 is the FDA 510(k) clearance record for R2 PADDLE TYPE CABLE-ADAPTOR #S 170,171, a class II device, cleared for R2 Corp. on under FDA product code LDD (Dc-Defibrillator, Low-Energy, (Including Paddles)). FDA records list 7 510(k) clearances for R2 Corp., from to . As of , FDA records show no recalls naming K800936.

Clearance record

Decision date
Received
(32 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
R2 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