Families of Master Neb, Primo Neb, SC03, Neb Aid, 4.2.NEB, Q03, FJ03, and Walkie-Neb

FDA 510(k) K062014 · Flaem Nuova S.P.A.

Substantially Equivalent

510(k) numberK062014

Submission

Device name
Families of Master Neb, Primo Neb, SC03, Neb Aid, 4.2.NEB, Q03, FJ03, and Walkie-Neb
Applicant
Flaem Nuova S.P.A.
North Reading, MA, US
Received
July 17, 2006
Decision date
March 22, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAF – Nebulizer (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5630
Specialty
Anesthesiology

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Questions and answers

When was Families of Master Neb, Primo Neb, SC03, Neb Aid, 4.2.NEB, Q03, FJ03, and Walkie-Neb cleared by the FDA?

Families of Master Neb, Primo Neb, SC03, Neb Aid, 4.2.NEB, Q03, FJ03, and Walkie-Neb (K062014) received a 510(k) decision of Substantially Equivalent on March 22, 2007, 248 days after the submission was received.

What is the product code of K062014?

The FDA product code is CAF – Nebulizer (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5630.