The following data is part of a premarket notification filed by Unipath Ltd. with the FDA for Turbox Fibrinogen.
| Device ID | K884179 |
| 510k Number | K884179 |
| Device Name: | TURBOX FIBRINOGEN |
| Classification | System, Fibrinogen Determination |
| Applicant | UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
| Contact | Mr. G Zajicek |
| Correspondent | Mr. G Zajicek UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
| Product Code | KQJ |
| CFR Regulation Number | 864.7340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-30 |
| Decision Date | 1988-12-20 |