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 |