510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K893609Substantially Equivalent

Teves Ecm (Endotracheal Cardiac Monitor)

Leonides Y. Teves, M.D., P.A., Bradenton FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893609 is the FDA 510(k) clearance record for TEVES ECM (ENDOTRACHEAL CARDIAC MONITOR), a class II device, cleared for Leonides Y. Teves, M.D., P.A. on under FDA product code BTR (Tube, Tracheal (W/Wo Connector)). FDA records list one 510(k) clearance for Leonides Y. Teves, M.D., P.A. As of , FDA records show no recalls naming K893609.

Clearance record

Decision date
Received
(173 days to decision)
Product code
BTR Tube, Tracheal (W/Wo Connector)
Regulation
21 CFR 868.5730
Device class
Class II
Review panel
Anesthesiology
Applicant
Leonides Y. Teves, M.D., P.A. The Palms Bldg., Bradenton FL
Third party review
No

Clearances, product code BTR

Trailing 12 months
2 clearances under product code BTR in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BTR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260