FDA 510(k)

Propeller Sensor for Neohaler

K-Number: K180770 · 2018-08-01

Decision Date2018-08-01

Product CodeCAF

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

Propeller Sensor for Neohaler is a medical device manufactured by Reciprocal Labs Corporation. It received FDA 510(k) clearance on 2018-08-01 under approval number K180770. 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 Propeller Sensor for Neohaler?

Propeller Sensor for Neohaler is a medical device that received FDA 510(k) clearance on 2018-08-01. It is manufactured by Reciprocal Labs Corporation. The 510(k) number is K180770.

When was Propeller Sensor for Neohaler approved by the FDA?

Propeller Sensor for Neohaler received FDA 510(k) clearance on 2018-08-01, under approval number K180770.

What company makes Propeller Sensor for Neohaler?

Propeller Sensor for Neohaler is manufactured by Reciprocal Labs Corporation.

What is the FDA product code for Propeller Sensor for Neohaler?

The FDA product code for Propeller Sensor for Neohaler is CAF.

Other Devices by Reciprocal Labs Corporation

K161454Propeller Sensor Model 2015-E K192724Propeller Sensor for Symbicort

Related Devices (Code: CAF)

K161454Propeller Sensor Model 2015-EReciprocal Labs Corporation K153010Hudson RCI AquaPak Sterile Prefilled NebulizersTeleflexmedical, Inc. K152882Propeller SystemReciprocal Labs K152482Propeller Sensor Model 2014-RReciprocal Labs K142541POCKET NEBMicrovaper Devices K170916Portable NebulizerMicrobase Technology Corporation

Official Source

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