The following data is part of a premarket notification filed by Organon Teknika Corp. with the FDA for Coag-a-mate Max.
| Device ID | K991101 |
| 510k Number | K991101 |
| Device Name: | COAG-A-MATE MAX |
| Classification | Instrument, Coagulation, Automated |
| Applicant | ORGANON TEKNIKA CORP. 100 AKZO AVE. Durham, NC 27712 |
| Contact | Rebecca A Rivas |
| Correspondent | Rebecca A Rivas ORGANON TEKNIKA CORP. 100 AKZO AVE. Durham, NC 27712 |
| Product Code | GKP |
| CFR Regulation Number | 864.5400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-04-01 |
| Decision Date | 1999-06-01 |
| Summary: | summary |