The following data is part of a premarket notification filed by Dayspring Medical, Inc. with the FDA for Blood Port Cap, Luer-lock Fitting, Dayspring Medical Part No. Bpc252ll.
Device ID | K961026 |
510k Number | K961026 |
Device Name: | BLOOD PORT CAP, LUER-LOCK FITTING, DAYSPRING MEDICAL PART NO. BPC252LL |
Classification | Dialyzer, Capillary, Hollow Fiber |
Applicant | DAYSPRING MEDICAL, INC. 1936 BEACON CT. Boulder, CO 80302 |
Contact | Neil Rasmussen |
Correspondent | Neil Rasmussen DAYSPRING MEDICAL, INC. 1936 BEACON CT. Boulder, CO 80302 |
Product Code | FJI |
CFR Regulation Number | 876.5820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-03-14 |
Decision Date | 1996-06-10 |