FDA 510(k)

CADWELL EASYNET NASAL PRESSURE MODULE

K-Number: K061705 · 2006-11-21

Decision Date2006-11-21

Product CodeMNR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CADWELL EASYNET NASAL PRESSURE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 2006-11-21 under 510(k) number K061705. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADWELL EASYNET NASAL PRESSURE MODULE?

CADWELL EASYNET NASAL PRESSURE MODULE is a medical device that received FDA 510(k) clearance on 2006-11-21. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K061705.

When did CADWELL EASYNET NASAL PRESSURE MODULE receive FDA 510(k) clearance?

CADWELL EASYNET NASAL PRESSURE MODULE received FDA 510(k) clearance on 2006-11-21, under 510(k) number K061705.

Who is the listed applicant for CADWELL EASYNET NASAL PRESSURE MODULE?

The FDA 510(k) record lists Cadwell Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CADWELL EASYNET NASAL PRESSURE MODULE?

The FDA product code for CADWELL EASYNET NASAL PRESSURE MODULE is MNR.

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Other records listing Cadwell Laboratories, Inc. as applicant

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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.