FDA 510(k)

POCKET NEB

K-Number: K142541 · 2016-01-22

Decision Date2016-01-22

Product CodeCAF

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

POCKET NEB is the device name listed in this FDA 510(k) record. The listed applicant is Microvaper Devices. It received FDA 510(k) clearance on 2016-01-22 under 510(k) 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. The listed applicant is Microvaper Devices. The 510(k) number is K142541.

When did POCKET NEB receive FDA 510(k) clearance?

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

Who is the listed applicant for POCKET NEB?

The FDA 510(k) record lists Microvaper Devices as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POCKET NEB?

The FDA product code for POCKET NEB is CAF.

Related Devices (Code: CAF)

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Official Source

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