The following data is part of a premarket notification filed by Teleflex, Inc. with the FDA for Conchasmart Breathing Circuit.
Device ID | K140556 |
510k Number | K140556 |
Device Name: | CONCHASMART BREATHING CIRCUIT |
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 | 2014-03-05 |
Decision Date | 2014-09-24 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
24026704553888 | K140556 | 000 |
24026704553840 | K140556 | 000 |
24026704553802 | K140556 | 000 |
24026704553789 | K140556 | 000 |
44026704553615 | K140556 | 000 |
40801902126533 | K140556 | 000 |
40801902126526 | K140556 | 000 |
40801902126519 | K140556 | 000 |