The following data is part of a premarket notification filed by Stoeckert Instrumente with the FDA for S3 Cyclic Rpm Control.
| Device ID | K971520 |
| 510k Number | K971520 |
| Device Name: | S3 CYCLIC RPM CONTROL |
| Classification | Pump, Blood, Cardiopulmonary Bypass, Roller Type |
| Applicant | STOECKERT INSTRUMENTE 49 PLAIN ST. North Attleboro, MA 02760 |
| Contact | Diane Minear |
| Correspondent | Diane Minear STOECKERT INSTRUMENTE 49 PLAIN ST. North Attleboro, MA 02760 |
| Product Code | DWB |
| CFR Regulation Number | 870.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-04-25 |
| Decision Date | 1997-09-10 |
| Summary: | summary |