510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K111050Substantially Equivalent

Esophageal / Rectal Temperature Probe, 9Fr, 12Fr, Esophageal Stethoscope with Temperature Sensor, 9Fr, 12Fr, 18Fr, 24Fr

Starboard Medical, Inc., Yorba Linda CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111050 is the FDA 510(k) clearance record for ESOPHAGEAL / RECTAL TEMPERATURE PROBE, 9FR, 12FR, ESOPHAGEAL STETHOSCOPE WITH TEMPERATURE SENSOR, 9FR, 12FR, 18FR, 24FR, a class II device, cleared for Starboard Medical, LLC on under FDA product code BZT (Stethoscope, Esophageal, With Electrical Conductors). FDA records list 3 510(k) clearances for Starboard Medical, LLC, from to . As of , FDA records show no recalls naming K111050.

Clearance record

Decision date
Received
(363 days to decision)
Product code
BZT Stethoscope, Esophageal, With Electrical Conductors
Regulation
21 CFR 868.1920
Device class
Class II
Review panel
Anesthesiology
Applicant
Starboard Medical, LLC 22845 Savi Ranch Pkwy. Suite H, Yorba Linda CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BZT

Trailing 12 months
1 clearance under product code BZT in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BZT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260