510(k) K874295

ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS by Sheridan Catheter Corp. — Product Code BZT

K874295 is an FDA 510(k) premarket notification submitted by Sheridan Catheter Corp. for the device "ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS". The FDA issued a decision of Substantially Equivalent on November 24, 1987. The device falls under product code BZT (Stethoscope, Esophageal, With Electrical Conductors), a Class II device regulated under 21 CFR 868.1920. Sheridan Catheter Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 24, 1987
Date Received
October 20, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stethoscope, Esophageal, With Electrical Conductors
Device Class
Class II
Regulation Number
868.1920
Review Panel
AN
Submission Type