The following data is part of a premarket notification filed by International Technidyne Corp. with the FDA for Hitt By Hemochron(r).
| Device ID | K910181 |
| 510k Number | K910181 |
| Device Name: | HITT BY HEMOCHRON(R) |
| Classification | Assay, Heparin |
| Applicant | INTERNATIONAL TECHNIDYNE CORP. 23 NEVSKY ST. Edison, NJ 08820 |
| Contact | Les Heimann |
| Correspondent | Les Heimann INTERNATIONAL TECHNIDYNE CORP. 23 NEVSKY ST. Edison, NJ 08820 |
| Product Code | KFF |
| CFR Regulation Number | 864.7525 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-01-16 |
| Decision Date | 1991-05-10 |