The following data is part of a premarket notification filed by Smiths Medical Ads, Inc. with the FDA for Bluselect, Non-fenestrated, Bluselect, Non-fenestrated, Cont, Bluselect, Fenestrated, Bluselect Suctionaid, Blupere Dilation Trachestomy Kit, Without Tube.
Device ID | K173384 |
510k Number | K173384 |
Device Name: | BLUselect, Non-fenestrated, BLUselect, Non-fenestrated, Cont, BLUselect, Fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, Without Tube |
Classification | Tube, Tracheostomy (w/wo Connector) |
Applicant | Smiths Medical ADS, Inc. 6000 Nathan Lane North Minneapolis, MN 55442 |
Contact | Donna M. Semlak |
Correspondent | Donna M. Semlak Smiths Medical ADS, Inc. 6000 Nathan Lane North Minneapolis, MN 55442 |
Product Code | BTO |
CFR Regulation Number | 868.5800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-10-30 |
Decision Date | 2018-04-10 |
Summary: | summary |