The following data is part of a premarket notification filed by Automated Iv Systems, Inc. with the FDA for Aiv Systems' Iv Poles.
Device ID | K895776 |
510k Number | K895776 |
Device Name: | AIV SYSTEMS' IV POLES |
Classification | Stand, Infusion |
Applicant | AUTOMATED IV SYSTEMS, INC. 200 DAVIS RD. Magnolia, NJ 08049 |
Contact | W. H Desjardins |
Correspondent | W. H Desjardins AUTOMATED IV SYSTEMS, INC. 200 DAVIS RD. Magnolia, NJ 08049 |
Product Code | FOX |
CFR Regulation Number | 880.6990 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-09-27 |
Decision Date | 1990-02-28 |