510(k) K844055

ESOPHAGEAL STETHO SCOPE by Sensortek, Inc. — Product Code BZT

K844055 is an FDA 510(k) premarket notification submitted by Sensortek, Inc. for the device "ESOPHAGEAL STETHO SCOPE". The FDA issued a decision of Substantially Equivalent on October 25, 1984. The device falls under product code BZT (Stethoscope, Esophageal, With Electrical Conductors), a Class II device regulated under 21 CFR 868.1920. Sensortek, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 1984
Date Received
October 18, 1984
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