510(k) K844055
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