510(k) K813143
K813143 is an FDA 510(k) premarket notification submitted by Exco, Inc. for the device "DESILET". The FDA issued a decision of Substantially Equivalent on November 27, 1981. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Exco, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 27, 1981
- Date Received
- November 5, 1981
- 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