510(k) K896203
K896203 is an FDA 510(k) premarket notification submitted by Solco Basle, Inc. for the device "SOLCOSEPT(TM) BLOOD TRANSFUSION FILTER". The FDA issued a decision of Substantially Equivalent on February 1, 1990. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Solco Basle, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 1, 1990
- Date Received
- October 26, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Microfilter, Blood Transfusion
- Device Class
- Class II
- Regulation Number
- 880.5440
- Review Panel
- HO
- Submission Type