The following data is part of a premarket notification filed by Sims Deltec, Inc. with the FDA for Cadd-legacy 1 Ambulatory Infusion System Model Number 6400.
Device ID | K982838 |
510k Number | K982838 |
Device Name: | CADD-LEGACY 1 AMBULATORY INFUSION SYSTEM MODEL NUMBER 6400 |
Classification | Pump, Infusion |
Applicant | SIMS DELTEC, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
Contact | Edward W Numainville |
Correspondent | Edward W Numainville SIMS DELTEC, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-08-12 |
Decision Date | 1998-11-04 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10610586019548 | K982838 | 000 |