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FDA 510(k)

MODEL LUNA MANUAL WHEELCHAIR

K-Number: K102910 · 2010-12-23

ApplicantP.D.G., Inc.
Decision Date2010-12-23
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL LUNA MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is P.D.G., Inc.. It received FDA 510(k) clearance on 2010-12-23 under 510(k) number K102910. 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 MODEL LUNA MANUAL WHEELCHAIR?

MODEL LUNA MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2010-12-23. The listed applicant is P.D.G., Inc.. The 510(k) number is K102910.

When did MODEL LUNA MANUAL WHEELCHAIR receive FDA 510(k) clearance?

MODEL LUNA MANUAL WHEELCHAIR received FDA 510(k) clearance on 2010-12-23, under 510(k) number K102910.

Who is the listed applicant for MODEL LUNA MANUAL WHEELCHAIR?

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

What is the FDA product code for MODEL LUNA MANUAL WHEELCHAIR?

The FDA product code for MODEL LUNA MANUAL WHEELCHAIR 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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