FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇿 New Zealand

ZEST NASAL MASK

K Number: K083832 · Decision Mar 16, 2009
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
449
Applicant Total
42
Review Days
83

Basic Information

Device Name
ZEST NASAL MASK
K Number
K083832
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
FISHER & PAYKEL HEALTHCARE, LTD.
Date Received
December 23, 2008
Decision Date
March 16, 2009
Product Code
BZD
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BZD Ventilator, Non-Continuous (Respirator)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BZD), ordered by most recent decision date.

View all

Other Clearances by FISHER & PAYKEL HEALTHCARE, LTD.

K Number Device Name
K132017 HC550 RESPIRATORY HUMIDIFIER, ADULT VENTILATOR CIRCUIT
K131957 MR810RESPIRATORY HUMIDIFIER, 900MR810 ADULT SINGLE LIMB CIRCUIT, 900MR810E ADULT DUAL LIMB CIRCUIT
K131895 AIRVO 2 HUMIDIFIER, MYAIRVO 2 HUMIDIFIER
K121975 AIRVO HUMIDIFIER MYAIRO HUMIDIFIER
K122432 ADULT EVAQUA 2' DUAL HEATED BREATHING CIRCUITS
K110019 RESPIRATORY HUMIDIFER
K110316 INFOSEND GSM
K103786 ZEST PETITE NASAL MASK
K100011 FISHER & PAYKEL HEALTHCARE BUBBLE CPAP SYSTEM
K100554 RESPIRATORY HUMIDIFIER , HEATED DELIVERY SYSTEM, ADAPTOR, MODELS MR880, RT241, 900MR441
Search all 42 clearances from FISHER & PAYKEL HEALTHCARE, LTD. →