Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR

K-Number: K051540 · 2005-09-21

ApplicantInovo, Inc.
Decision Date2005-09-21
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Inovo, Inc.. It received FDA 510(k) clearance on 2005-09-21 under 510(k) number K051540. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR?

INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR is a medical device that received FDA 510(k) clearance on 2005-09-21. The listed applicant is Inovo, Inc.. The 510(k) number is K051540.

When did INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR receive FDA 510(k) clearance?

INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR received FDA 510(k) clearance on 2005-09-21, under 510(k) number K051540.

Who is the listed applicant for INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR?

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

What is the FDA product code for INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR?

The FDA product code for INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR is NFB.

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 Inovo, 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.

Related Devices (Code: NFB)

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.

↑