The following data is part of a premarket notification filed by R & D Systems, Inc. with the FDA for Csf Automated Control, Models Csf001, Csf003.
Device ID | K072846 |
510k Number | K072846 |
Device Name: | CSF AUTOMATED CONTROL, MODELS CSF001, CSF003 |
Classification | Mixture, Hematology Quality Control |
Applicant | R & D SYSTEMS, INC. 614 MCKINLEY PL., N.E. Minneapolis, MN 55413 |
Contact | Nancy C Ring |
Correspondent | Nancy C Ring R & D SYSTEMS, INC. 614 MCKINLEY PL., N.E. Minneapolis, MN 55413 |
Product Code | JPK |
CFR Regulation Number | 864.8625 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-10-04 |
Decision Date | 2007-11-26 |
Summary: | summary |