510(k) K864890
K864890 is an FDA 510(k) premarket notification submitted by Shiley, Inc. for the device "STOCKERT-SHILEY CAPS VENOUS OCCLUSION CLAMP". The FDA issued a decision of Substantially Equivalent on February 19, 1987. The device falls under product code KRI (Accessory Equipment, Cardiopulmonary Bypass), a Class I device regulated under 21 CFR 870.4200. Shiley, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 19, 1987
- Date Received
- December 15, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accessory Equipment, Cardiopulmonary Bypass
- Device Class
- Class I
- Regulation Number
- 870.4200
- Review Panel
- CV
- Submission Type