The following data is part of a premarket notification filed by Sims Deltec, Inc. with the FDA for Deltec Subcutaneous Infusion Set.
| Device ID | K963009 |
| 510k Number | K963009 |
| Device Name: | DELTEC SUBCUTANEOUS INFUSION SET |
| Classification | Set, Administration, Intravascular |
| Applicant | SIMS DELTEC, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
| Contact | David H Short, Rn,bs |
| Correspondent | David H Short, Rn,bs SIMS DELTEC, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-08-02 |
| Decision Date | 1996-10-18 |
| Summary: | summary |