The following data is part of a premarket notification filed by Hospal Medical Corp. with the FDA for Model H 607-.67m2 30 Micron Rp An69 Mem.
| Device ID | K800536 |
| 510k Number | K800536 |
| Device Name: | MODEL H 607-.67M2 30 MICRON RP AN69 MEM |
| Classification | Dialyzer, High Permeability With Or Without Sealed Dialysate System |
| Applicant | HOSPAL MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KDI |
| CFR Regulation Number | 876.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-03-10 |
| Decision Date | 1980-08-07 |