The following data is part of a premarket notification filed by Sartorius Filters, Inc. with the FDA for Sartorius Mini Sart Fh 16592.
Device ID | K851818 |
510k Number | K851818 |
Device Name: | SARTORIUS MINI SART FH 16592 |
Classification | Filter, Infusion Line |
Applicant | SARTORIUS FILTERS, INC. 30940 SAN CLEMENTE ST. Hayward, CA 94544 |
Contact | Steven Cates |
Correspondent | Steven Cates SARTORIUS FILTERS, INC. 30940 SAN CLEMENTE ST. Hayward, CA 94544 |
Product Code | FPB |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-26 |
Decision Date | 1985-08-19 |