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FDA 510(k)

MCC-MIV ONE 2 ONE SOFTWARE

K-Number: K010364 · 2001-03-22

Decision Date2001-03-22
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MCC-MIV ONE 2 ONE SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2001-03-22 under 510(k) number K010364. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCC-MIV ONE 2 ONE SOFTWARE?

MCC-MIV ONE 2 ONE SOFTWARE is a medical device that received FDA 510(k) clearance on 2001-03-22. The listed applicant is Invacare Corp.. The 510(k) number is K010364.

When did MCC-MIV ONE 2 ONE SOFTWARE receive FDA 510(k) clearance?

MCC-MIV ONE 2 ONE SOFTWARE received FDA 510(k) clearance on 2001-03-22, under 510(k) number K010364.

Who is the listed applicant for MCC-MIV ONE 2 ONE SOFTWARE?

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 MCC-MIV ONE 2 ONE SOFTWARE?

The FDA product code for MCC-MIV ONE 2 ONE SOFTWARE is ITI.

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: ITI)

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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