510(k) K873667
K873667 is an FDA 510(k) premarket notification submitted by Pall Biomedical Products Co. for the device "PALL LEUKOCYTE REMOVAL FILTER, PLATELETS". The FDA issued a decision of Substantially Equivalent on January 6, 1988. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Pall Biomedical Products Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 6, 1988
- Date Received
- September 10, 1987
- 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