510(k) K901887
K901887 is an FDA 510(k) premarket notification submitted by Asahi Medical Co., Ltd. for the device "MODIFIED SEPACELL R-SERIES BLOOD FILTERS". The FDA issued a decision of Substantially Equivalent on August 8, 1990. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Asahi Medical Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 8, 1990
- Date Received
- April 26, 1990
- 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