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FDA 510(k)

Propeller Sensor for Symbicort

K-Number: K192724 · 2020-03-26

ApplicantReciprocal Labs Corporation
Decision Date2020-03-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Propeller Sensor for Symbicort is the device name listed in this FDA 510(k) record. The listed applicant is Reciprocal Labs Corporation. It received FDA 510(k) clearance on 2020-03-26 under 510(k) number K192724. 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 Symbicort?

Propeller Sensor for Symbicort is a medical device that received FDA 510(k) clearance on 2020-03-26. The listed applicant is Reciprocal Labs Corporation. The 510(k) number is K192724.

When did Propeller Sensor for Symbicort receive FDA 510(k) clearance?

Propeller Sensor for Symbicort received FDA 510(k) clearance on 2020-03-26, under 510(k) number K192724.

Who is the listed applicant for Propeller Sensor for Symbicort?

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

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

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

Other records listing Reciprocal Labs Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: CAF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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