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FDA 510(k)

7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L

K-Number: K061273 · 2006-05-23

ApplicantNova Ortho-Med, Inc.
Decision Date2006-05-23
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L is the device name listed in this FDA 510(k) record. The listed applicant is Nova Ortho-Med, Inc.. It received FDA 510(k) clearance on 2006-05-23 under 510(k) number K061273. 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 7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L?

7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L is a medical device that received FDA 510(k) clearance on 2006-05-23. The listed applicant is Nova Ortho-Med, Inc.. The 510(k) number is K061273.

When did 7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L receive FDA 510(k) clearance?

7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L received FDA 510(k) clearance on 2006-05-23, under 510(k) number K061273.

Who is the listed applicant for 7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L?

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

What is the FDA product code for 7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L?

The FDA product code for 7000 SERIES LIGHTWEIGHT WHEELCHAIR, MODELS 7160L, 7180L AND 7200L is IOR.

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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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