The following data is part of a premarket notification filed by Icu Medical, Inc. with the FDA for Clave Connector.
Device ID | K915571 |
510k Number | K915571 |
Device Name: | CLAVE CONNECTOR |
Classification | Set, Administration, Intravascular |
Applicant | ICU MEDICAL, INC. 142 TECHNOLOGY DR. Irvine, CA 92718 |
Contact | Araceli C.fancher |
Correspondent | Araceli C.fancher 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 | 1991-12-12 |
Decision Date | 1992-09-21 |