The following data is part of a premarket notification filed by Top Surgical Manufacturers Co. with the FDA for Top Three Way Stopcock.
| Device ID | K832625 |
| 510k Number | K832625 |
| Device Name: | TOP THREE WAY STOPCOCK |
| Classification | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
| Applicant | TOP SURGICAL MANUFACTURERS CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DTL |
| CFR Regulation Number | 870.4290 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-04 |
| Decision Date | 1983-10-19 |