The following data is part of a premarket notification filed by Icu Medical, Inc. with the FDA for Safe Connector.
Device ID | K940296 |
510k Number | K940296 |
Device Name: | SAFE CONNECTOR |
Classification | Set, Administration, Intravascular |
Applicant | ICU MEDICAL, INC. 142 TECHNOLOGY DR. Irvine, CA 92718 |
Contact | Salvadore F Palomares |
Correspondent | Salvadore F Palomares ICU MEDICAL, INC. 142 TECHNOLOGY DR. Irvine, CA 92718 |
Product Code | FPA |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-01-21 |
Decision Date | 1994-02-22 |