510(k) K823259
K823259 is an FDA 510(k) premarket notification submitted by Medical, Inc. for the device "INTERFACE CARDIOTOMY BLOOD FILTER #50". The FDA issued a decision of Substantially Equivalent on November 24, 1982. The device falls under product code JOD (Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4270. Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 24, 1982
- Date Received
- November 2, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4270
- Review Panel
- CV
- Submission Type