510(k) K072846
K072846 is an FDA 510(k) premarket notification submitted by R&D Systems, Inc. for the device "CSF AUTOMATED CONTROL, MODELS CSF001, CSF003". The FDA issued a decision of Substantially Equivalent on November 26, 2007. The device falls under product code JPK (Mixture, Hematology Quality Control), a Class II device regulated under 21 CFR 864.8625. R&D Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 26, 2007
- Date Received
- October 4, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mixture, Hematology Quality Control
- Device Class
- Class II
- Regulation Number
- 864.8625
- Review Panel
- HE
- Submission Type