510(k) K830218

SHERIDAN/ESOPHAGEAL STETHOSCOPE by Sheridan Catheter Corp. — Product Code BZW

K830218 is an FDA 510(k) premarket notification submitted by Sheridan Catheter Corp. for the device "SHERIDAN/ESOPHAGEAL STETHOSCOPE". The FDA issued a decision of Substantially Equivalent on March 9, 1983. The device falls under product code BZW (Stethoscope, Esophageal), a Class I device regulated under 21 CFR 868.1910. Sheridan Catheter Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 9, 1983
Date Received
January 24, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stethoscope, Esophageal
Device Class
Class I
Regulation Number
868.1910
Review Panel
AN
Submission Type