510(k) K881293
K881293 is an FDA 510(k) premarket notification submitted by Sheridan Catheter Corp. for the device "SHERIDAN ELECTROSURGERY PROTECTION FILTER". The FDA issued a decision of Substantially Equivalent on June 16, 1988. 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
- June 16, 1988
- Date Received
- March 28, 1988
- 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