The following data is part of a premarket notification filed by International Technidyne Corp. with the FDA for Hemochron/factor Vi Fibrinogen Assay And Cont Plas.
| Device ID | K923593 |
| 510k Number | K923593 |
| Device Name: | HEMOCHRON/FACTOR VI FIBRINOGEN ASSAY AND CONT PLAS |
| Classification | System, Fibrinogen Determination |
| Applicant | INTERNATIONAL TECHNIDYNE CORP. 23 NEVSKY ST. Edison, NJ 08820 |
| Contact | Matt Lesnieski |
| Correspondent | Matt Lesnieski INTERNATIONAL TECHNIDYNE CORP. 23 NEVSKY ST. Edison, NJ 08820 |
| Product Code | KQJ |
| CFR Regulation Number | 864.7340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-07-20 |
| Decision Date | 1992-09-22 |