The following data is part of a premarket notification filed by Fisher & Paykel Allied Products Ltd. with the FDA for Heated Respiratory Humidifier.
Device ID | K851879 |
510k Number | K851879 |
Device Name: | HEATED RESPIRATORY HUMIDIFIER |
Classification | Humidifier, Respiratory Gas, (direct Patient Interface) |
Applicant | FISHER & PAYKEL ALLIED PRODUCTS LTD. 25 CARBINE ROAD, PANMURE P.O. BOX 14-348, PANMURE Auckland, New Zealand, NZ |
Contact | David Milburn |
Correspondent | David Milburn FISHER & PAYKEL ALLIED PRODUCTS LTD. 25 CARBINE ROAD, PANMURE P.O. BOX 14-348, PANMURE Auckland, New Zealand, NZ |
Product Code | BTT |
CFR Regulation Number | 868.5450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-29 |
Decision Date | 1985-09-03 |