510(k) K942844
K942844 is an FDA 510(k) premarket notification submitted by Level 1 Technologies, Inc. for the device "LEVEL 1 BLOOD STREAM RECOVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on April 26, 1996. The device falls under product code CAC (Apparatus, Autotransfusion), a Class II device regulated under 21 CFR 868.5830. Level 1 Technologies, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 26, 1996
- Date Received
- June 16, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Apparatus, Autotransfusion
- Device Class
- Class II
- Regulation Number
- 868.5830
- Review Panel
- CV
- Submission Type