510(k) K881293

SHERIDAN ELECTROSURGERY PROTECTION FILTER by Sheridan Catheter Corp. — Product Code BZT

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