The following data is part of a premarket notification filed by Hospal Medical Corp. with the FDA for Hospal Biospal 1800s.
Device ID | K863961 |
510k Number | K863961 |
Device Name: | HOSPAL BIOSPAL 1800S |
Classification | Dialyzer, High Permeability With Or Without Sealed Dialysate System |
Applicant | HOSPAL MEDICAL CORP. 25 KIMBERLY RD. P.O. BOX 857 East Brunswick, NJ 08816 |
Contact | Catherina Madormo |
Correspondent | Catherina Madormo HOSPAL MEDICAL CORP. 25 KIMBERLY RD. P.O. BOX 857 East Brunswick, NJ 08816 |
Product Code | KDI |
CFR Regulation Number | 876.5860 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-10-10 |
Decision Date | 1986-12-17 |