The following data is part of a premarket notification filed by International Technidyne Corp. with the FDA for Hemochron(r) Aptt, Modification.
| Device ID | K911994 |
| 510k Number | K911994 |
| Device Name: | HEMOCHRON(R) APTT, MODIFICATION |
| Classification | Activated Partial Thromboplastin |
| 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 | GFO |
| CFR Regulation Number | 864.7925 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-04-22 |
| Decision Date | 1991-07-17 |