The following data is part of a premarket notification filed by Bio Medicus, Inc. with the FDA for Bio Medicus Bio Pump Model Bp-50.
| Device ID | K852807 |
| 510k Number | K852807 |
| Device Name: | BIO MEDICUS BIO PUMP MODEL BP-50 |
| Classification | Pump, Blood, Cardiopulmonary Bypass, Non-roller Type |
| Applicant | BIO MEDICUS, INC. 9600 W. 76 ST. Eden Prairie, MN 55344 |
| Contact | John R Dalpee |
| Correspondent | John R Dalpee BIO MEDICUS, INC. 9600 W. 76 ST. Eden Prairie, MN 55344 |
| Product Code | KFM |
| CFR Regulation Number | 870.4360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-07-02 |
| Decision Date | 1985-09-30 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20613994406938 | K852807 | 000 |
| 20643169794775 | K852807 | 000 |
| 00643169630604 | K852807 | 000 |