The following data is part of a premarket notification filed by Jostra Ag with the FDA for Jostra Suckers, Model Js.
| Device ID | K020983 |
| 510k Number | K020983 |
| Device Name: | JOSTRA SUCKERS, MODEL JS |
| Classification | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Applicant | JOSTRA AG 478 MEDIA RD. Oxford, PA 19363 |
| Contact | Kathleen Johnson |
| Correspondent | Kathleen Johnson JOSTRA AG 478 MEDIA RD. Oxford, PA 19363 |
| Product Code | DWF |
| CFR Regulation Number | 870.4210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-27 |
| Decision Date | 2004-01-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04037691127941 | K020983 | 000 |
| 04037691064147 | K020983 | 000 |
| 04037691401331 | K020983 | 000 |
| 04037691141978 | K020983 | 000 |