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FDA 510(k)

RUNCH INDUSTRIAL WHEELCHAIR

K-Number: K980107 · 1998-02-19

ApplicantRunch Group USA, Inc.
Decision Date1998-02-19
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RUNCH INDUSTRIAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Runch Group USA, Inc.. It received FDA 510(k) clearance on 1998-02-19 under 510(k) number K980107. 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 RUNCH INDUSTRIAL WHEELCHAIR?

RUNCH INDUSTRIAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1998-02-19. The listed applicant is Runch Group USA, Inc.. The 510(k) number is K980107.

When did RUNCH INDUSTRIAL WHEELCHAIR receive FDA 510(k) clearance?

RUNCH INDUSTRIAL WHEELCHAIR received FDA 510(k) clearance on 1998-02-19, under 510(k) number K980107.

Who is the listed applicant for RUNCH INDUSTRIAL WHEELCHAIR?

The FDA 510(k) record lists Runch Group USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUNCH INDUSTRIAL WHEELCHAIR?

The FDA product code for RUNCH INDUSTRIAL 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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