The following data is part of a premarket notification filed by Delmed, Inc. with the FDA for Freedom Set Ii With Triflex Valve.
Device ID | K870626 |
510k Number | K870626 |
Device Name: | FREEDOM SET II WITH TRIFLEX VALVE |
Classification | Set, Administration, For Peritoneal Dialysis, Disposable |
Applicant | DELMED, INC. P.O. DRAWER 190 Freehold, NJ 07728 |
Contact | A. P Doerschuck |
Correspondent | A. P Doerschuck DELMED, INC. P.O. DRAWER 190 Freehold, NJ 07728 |
Product Code | KDJ |
CFR Regulation Number | 876.5630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-02-13 |
Decision Date | 1987-06-03 |