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FDA 510(k)

RESPICHAMBER VALVED HOLDING CHAMBER

K-Number: K110136 · 2011-04-18

Decision Date2011-04-18
Product CodeNVP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPICHAMBER VALVED HOLDING CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is Trudell Medical Intl.. It received FDA 510(k) clearance on 2011-04-18 under 510(k) number K110136. The device is classified under product code NVP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPICHAMBER VALVED HOLDING CHAMBER?

RESPICHAMBER VALVED HOLDING CHAMBER is a medical device that received FDA 510(k) clearance on 2011-04-18. The listed applicant is Trudell Medical Intl.. The 510(k) number is K110136.

When did RESPICHAMBER VALVED HOLDING CHAMBER receive FDA 510(k) clearance?

RESPICHAMBER VALVED HOLDING CHAMBER received FDA 510(k) clearance on 2011-04-18, under 510(k) number K110136.

Who is the listed applicant for RESPICHAMBER VALVED HOLDING CHAMBER?

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

What is the FDA product code for RESPICHAMBER VALVED HOLDING CHAMBER?

The FDA product code for RESPICHAMBER VALVED HOLDING CHAMBER is NVP.

Related Clinical Trials

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.

Other records listing Trudell Medical Intl. 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.

View all 12 devices →

Related Devices (Code: NVP)

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.

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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