The following data is part of a premarket notification filed by Critikon Company,llc with the FDA for Critikon I.v. Filter.
Device ID | K842075 |
510k Number | K842075 |
Device Name: | CRITIKON I.V. FILTER |
Classification | Filter, Infusion Line |
Applicant | CRITIKON COMPANY,LLC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | FPB |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-05-23 |
Decision Date | 1984-06-28 |