510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K895110Substantially Equivalent

Maestro Pacemaker Test Magnet

Cardiac Control Systems, Inc., Palm Coast FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895110 is the FDA 510(k) clearance record for MAESTRO PACEMAKER TEST MAGNET, a class I device, cleared for Cardiac Control Systems, Inc. on under FDA product code DTG (Magnet, Test, Pacemaker). FDA records list 26 510(k) clearances for Cardiac Control Systems, Inc., from to . As of , FDA records show no recalls naming K895110.

Clearance record

Decision date
Received
(42 days to decision)
Product code
DTG Magnet, Test, Pacemaker
Regulation
21 CFR 870.3690
Device class
Class I
Review panel
Cardiovascular
Applicant
Cardiac Control Systems, Inc. 3 Commerce Blvd., Palm Coast FL
Third party review
No

Clearances, product code DTG

Trailing 12 months

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

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