The following data is part of a premarket notification filed by Respironics, Inc. with the FDA for Ti Nasal Mask.
Device ID | K140980 |
510k Number | K140980 |
Device Name: | TI NASAL MASK |
Classification | Ventilator, Non-continuous (respirator) |
Applicant | RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
Contact | Shaylee Masilunas |
Correspondent | Shaylee Masilunas RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
Product Code | BZD |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-04-16 |
Decision Date | 2015-02-10 |
Summary: | summary |