The following data is part of a premarket notification filed by Stedim, Inc. with the FDA for Automix Compounder Y - Adaptor Set.
Device ID | K890205 |
510k Number | K890205 |
Device Name: | AUTOMIX COMPOUNDER Y - ADAPTOR SET |
Classification | Set, I.v. Fluid Transfer |
Applicant | STEDIM, INC. 3667 PERADA DR. Walnut Creek, CA 94598 |
Contact | Bryan L Krause |
Correspondent | Bryan L Krause STEDIM, INC. 3667 PERADA DR. Walnut Creek, CA 94598 |
Product Code | LHI |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-01-18 |
Decision Date | 1989-10-27 |