510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K831977Substantially Equivalent

C Tec Series 9000 e.c.g. Electrode

Speywood Medical, Ltd., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831977 is the FDA 510(k) clearance record for C TEC SERIES 9000 E.C.G. ELECTRODE, a class II device, cleared for Speywood Medical, Ltd. on under FDA product code DRX (Electrode, Electrocardiograph). FDA records list one 510(k) clearance for Speywood Medical, Ltd. As of , FDA records show no recalls naming K831977.

Clearance record

Decision date
Received
(81 days to decision)
Product code
DRX Electrode, Electrocardiograph
Regulation
21 CFR 870.2360
Device class
Class II
Review panel
Cardiovascular
Applicant
Speywood Medical, Ltd. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DRX

Trailing 12 months

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

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