510(k) K830218
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