The following data is part of a premarket notification filed by International Technidyne Corp. with the FDA for Catalog No. J-act+ & Qc-act+.
| Device ID | K941007 |
| 510k Number | K941007 |
| Device Name: | CATALOG NO. J-ACT+ & QC-ACT+ |
| Classification | Activated Whole Blood Clotting Time |
| Applicant | INTERNATIONAL TECHNIDYNE CORP. 23 NEVSKY ST. Edison, NJ 08820 |
| Contact | Robert N Borghese |
| Correspondent | Robert N Borghese INTERNATIONAL TECHNIDYNE CORP. 23 NEVSKY ST. Edison, NJ 08820 |
| Product Code | JBP |
| CFR Regulation Number | 864.7140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-03-01 |
| Decision Date | 1994-06-30 |