The following data is part of a premarket notification filed by Medisystems Corp. with the FDA for Medisystems Dialysis Priming Sets.
Device ID | K971860 |
510k Number | K971860 |
Device Name: | MEDISYSTEMS DIALYSIS PRIMING SETS |
Classification | Accessories, Blood Circuit, Hemodialysis |
Applicant | MEDISYSTEMS CORP. 1900 K STREET, N.W. Washington, DC 20006 |
Contact | Larry R Pilot |
Correspondent | Larry R Pilot MEDISYSTEMS CORP. 1900 K STREET, N.W. Washington, DC 20006 |
Product Code | KOC |
CFR Regulation Number | 876.5820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-05-20 |
Decision Date | 1997-08-18 |
Summary: | summary |