510(k) K792170
K792170 is an FDA 510(k) premarket notification submitted by Stanco Medical, Inc. for the device "PERCUTANEOUS SHEATH (MULTI-CATH)SIDE". The FDA issued a decision of Substantially Equivalent on November 13, 1979. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Stanco Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 13, 1979
- Date Received
- October 29, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Introducer, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1340
- Review Panel
- CV
- Submission Type