The following data is part of a premarket notification filed by Seracare Technology with the FDA for Urine Drug Screening Control.
| Device ID | K992395 |
| 510k Number | K992395 |
| Device Name: | URINE DRUG SCREENING CONTROL |
| Classification | Drug Mixture Control Materials |
| Applicant | SERACARE TECHNOLOGY 2170 WOODWARD ST. Austin, TX 78744 -1832 |
| Contact | Rusty Sewell |
| Correspondent | Rusty Sewell SERACARE TECHNOLOGY 2170 WOODWARD ST. Austin, TX 78744 -1832 |
| Product Code | DIF |
| CFR Regulation Number | 862.3280 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-19 |
| Decision Date | 1999-08-26 |
| Summary: | summary |