FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

MC 300* Nebulizer

K Number: K173367 · Decision Feb 28, 2018
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
9
Review Days
125

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MC 300* Nebulizer
K Number
K173367
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Trudell Medical International
Date Received
October 26, 2017
Decision Date
February 28, 2018
Product Code
CAF
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
CAF Nebulizer (Direct Patient Interface)

Similar 510(k) Clearances

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

View all

Other Clearances by Trudell Medical International

K Number Device Name
K242667 AeroChamber2go Anti-Static Valved Holding Chamber
K203400 Corrugated tube with mouthpiece accessory
K200063 AeroEclipse* ONE BAN
K183108 Combined Aerobika OPEP and VersaPAP device
K181649 AeroChamber Plus* Flow-Vu* Anti-Static Valved Holding Chamber (VHC)
K173918 VersaPAP Positive Airway Pressure (PAP) Device
K173825 MC 300R* Nebulizer
K150173 Aerobika OPEP Devive with Manometer