The following data is part of a premarket notification filed by Fisher & Paykel Healthcare, Ltd. with the FDA for Zest Petite Nasal Mask.
Device ID | K103786 |
510k Number | K103786 |
Device Name: | ZEST PETITE NASAL MASK |
Classification | Ventilator, Non-continuous (respirator) |
Applicant | FISHER & PAYKEL HEALTHCARE, LTD. 15 MAURICE PAYKEL PLACE East Tamaki, Auckland, NZ 2013 |
Contact | Tina Mason |
Correspondent | Tina Mason FISHER & PAYKEL HEALTHCARE, LTD. 15 MAURICE PAYKEL PLACE East Tamaki, Auckland, NZ 2013 |
Product Code | BZD |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-12-27 |
Decision Date | 2011-03-24 |
Summary: | summary |