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FDA 510(k)

MODEL IPD OXYGEN CONSERVING DEVICE

K-Number: K953852 · 1995-11-22

Decision Date1995-11-22
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL IPD OXYGEN CONSERVING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1995-11-22 under 510(k) number K953852. 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 MODEL IPD OXYGEN CONSERVING DEVICE?

MODEL IPD OXYGEN CONSERVING DEVICE is a medical device that received FDA 510(k) clearance on 1995-11-22. The listed applicant is Invacare Corp.. The 510(k) number is K953852.

When did MODEL IPD OXYGEN CONSERVING DEVICE receive FDA 510(k) clearance?

MODEL IPD OXYGEN CONSERVING DEVICE received FDA 510(k) clearance on 1995-11-22, under 510(k) number K953852.

Who is the listed applicant for MODEL IPD OXYGEN CONSERVING DEVICE?

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

What is the FDA product code for MODEL IPD OXYGEN CONSERVING DEVICE?

The FDA product code for MODEL IPD OXYGEN CONSERVING DEVICE 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 Invacare Corp. 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 111 devices →

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.

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