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FDA 510(k)

RTM AND OVAL

K-Number: K080880 · 2008-04-09

ApplicantNext Mobility, LLC
Decision Date2008-04-09
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RTM AND OVAL is the device name listed in this FDA 510(k) record. The listed applicant is Next Mobility, LLC. It received FDA 510(k) clearance on 2008-04-09 under 510(k) number K080880. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RTM AND OVAL?

RTM AND OVAL is a medical device that received FDA 510(k) clearance on 2008-04-09. The listed applicant is Next Mobility, LLC. The 510(k) number is K080880.

When did RTM AND OVAL receive FDA 510(k) clearance?

RTM AND OVAL received FDA 510(k) clearance on 2008-04-09, under 510(k) number K080880.

Who is the listed applicant for RTM AND OVAL?

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

What is the FDA product code for RTM AND OVAL?

The FDA product code for RTM AND OVAL is IOR.

Other records listing Next Mobility, LLC 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.

K081665MILLENIUM II

Related Devices (Code: IOR)

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.

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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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