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FDA 510(k)

POCKET NEB

K-Number: K142541 · 2016-01-22

ApplicantMicrovaper Devices
Decision Date2016-01-22
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POCKET NEB is a medical device manufactured by Microvaper Devices. It received FDA 510(k) clearance on 2016-01-22 under approval number K142541. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POCKET NEB?

POCKET NEB is a medical device that received FDA 510(k) clearance on 2016-01-22. It is manufactured by Microvaper Devices. The 510(k) number is K142541.

When was POCKET NEB approved by the FDA?

POCKET NEB received FDA 510(k) clearance on 2016-01-22, under approval number K142541.

What company makes POCKET NEB?

POCKET NEB is manufactured by Microvaper Devices.

What is the FDA product code for POCKET NEB?

The FDA product code for POCKET NEB is CAF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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