The following data is part of a premarket notification filed by Teleflex, Inc. with the FDA for Conchasmart Column.
| Device ID | K141940 |
| 510k Number | K141940 |
| Device Name: | CONCHASMART COLUMN |
| Classification | Humidifier, Respiratory Gas, (direct Patient Interface) |
| Applicant | TELEFLEX, INC. 2917 WECK DR. Research Triangle Park, NC 27709 |
| Contact | Amanda Webb |
| Correspondent | Amanda Webb TELEFLEX, INC. 2917 WECK DR. Research Triangle Park, NC 27709 |
| Product Code | BTT |
| CFR Regulation Number | 868.5450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-07-17 |
| Decision Date | 2014-11-24 |
| Summary: | summary |