510(k) K823261
K823261 is an FDA 510(k) premarket notification submitted by Medical, Inc. for the device "INTERFACE TRANSFUSION BLOOD FILTER #30". The FDA issued a decision of Substantially Equivalent on January 7, 1983. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 7, 1983
- Date Received
- November 2, 1982
- 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