510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830218Substantially Equivalent

Sheridan/esophageal Stethoscope

Sheridan Catheter Corp., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830218 is the FDA 510(k) clearance record for SHERIDAN/ESOPHAGEAL STETHOSCOPE, a class I device, cleared for Sheridan Catheter Corp. on under FDA product code BZW (Stethoscope, Esophageal). FDA records list 39 510(k) clearances for Sheridan Catheter Corp., from to . As of , FDA records show no recalls naming K830218.

Clearance record

Decision date
Received
(44 days to decision)
Product code
BZW Stethoscope, Esophageal
Regulation
21 CFR 868.1910
Device class
Class I
Review panel
Anesthesiology
Applicant
Sheridan Catheter Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code BZW

Trailing 12 months

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

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