510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110192Substantially Equivalent

Defibrillator Analyzer - Da-2006P

BC Group International Inc, Oak Grove MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110192 is the FDA 510(k) clearance record for DEFIBRILLATOR ANALYZER - DA-2006P, a class II device, cleared for Bc Group International, Inc. on under FDA product code DRL (Tester, Defibrillator). FDA records list 2 510(k) clearances for Bc Group International, Inc., from to . As of , FDA records show one recall naming K110192.

Clearance record

Decision date
Received
(15 days to decision)
Product code
DRL Tester, Defibrillator
Regulation
21 CFR 870.5325
Device class
Class II
Review panel
Cardiovascular
Applicant
Bc Group International, Inc. 2913, 209th Ln. NW, Oak Grove MN
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code DRL

Trailing 12 months

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

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