The following data is part of a premarket notification filed by Beckman Coulter, Inc. with the FDA for Synchron Systems Dat Low And High Urine Controls 1.
| Device ID | K983709 |
| 510k Number | K983709 |
| Device Name: | SYNCHRON SYSTEMS DAT LOW AND HIGH URINE CONTROLS 1 |
| Classification | Drug Mixture Control Materials |
| Applicant | BECKMAN COULTER, INC. 200 S. KRAEMER BLVD.,M/S W-104 BOX 8000 Brea, CA 92822 -8000 |
| Contact | Lucinda Stockert |
| Correspondent | Lucinda Stockert BECKMAN COULTER, INC. 200 S. KRAEMER BLVD.,M/S W-104 BOX 8000 Brea, CA 92822 -8000 |
| Product Code | DIF |
| CFR Regulation Number | 862.3280 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-10-21 |
| Decision Date | 1998-10-28 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15099590223328 | K983709 | 000 |
| 15099590223311 | K983709 | 000 |