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FDA 510(k)

PROVENT NASAL CANNULA

K-Number: K080983 · 2008-08-07

ApplicantVentus Medical, Inc.
Decision Date2008-08-07
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PROVENT NASAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Ventus Medical, Inc.. It received FDA 510(k) clearance on 2008-08-07 under 510(k) number K080983. 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 PROVENT NASAL CANNULA?

PROVENT NASAL CANNULA is a medical device that received FDA 510(k) clearance on 2008-08-07. The listed applicant is Ventus Medical, Inc.. The 510(k) number is K080983.

When did PROVENT NASAL CANNULA receive FDA 510(k) clearance?

PROVENT NASAL CANNULA received FDA 510(k) clearance on 2008-08-07, under 510(k) number K080983.

Who is the listed applicant for PROVENT NASAL CANNULA?

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

What is the FDA product code for PROVENT NASAL CANNULA?

The FDA product code for PROVENT NASAL CANNULA is MNR.

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Other records listing Ventus Medical, Inc. 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.

K120665INVENT SNORING DEVICEK102404PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50)K090398PROVENT PROFESSIONAL SLEEP APNEA THERAPYK071560PROVENT NASAL DILATOR, MODEL BR2

Related Devices (Code: MNR)

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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.

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