The following data is part of a premarket notification filed by Resmed Ltd. with the FDA for Nasal Jacks Mask.
Device ID | K032433 |
510k Number | K032433 |
Device Name: | NASAL JACKS MASK |
Classification | Ventilator, Non-continuous (respirator) |
Applicant | RESMED LTD. 14040 DANIELSON ST. Poway, CA 92064 -6857 |
Contact | David D'cruz |
Correspondent | David D'cruz RESMED LTD. 14040 DANIELSON ST. Poway, CA 92064 -6857 |
Product Code | BZD |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-08-06 |
Decision Date | 2003-10-24 |
Summary: | summary |