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FDA 510(k)

HI-RIDER WHEELCHAIR

K-Number: K890695 · 1989-04-10

ApplicantRetec USA, Inc.
Decision Date1989-04-10
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HI-RIDER WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Retec USA, Inc.. It received FDA 510(k) clearance on 1989-04-10 under 510(k) number K890695. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HI-RIDER WHEELCHAIR?

HI-RIDER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1989-04-10. The listed applicant is Retec USA, Inc.. The 510(k) number is K890695.

When did HI-RIDER WHEELCHAIR receive FDA 510(k) clearance?

HI-RIDER WHEELCHAIR received FDA 510(k) clearance on 1989-04-10, under 510(k) number K890695.

Who is the listed applicant for HI-RIDER WHEELCHAIR?

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

What is the FDA product code for HI-RIDER WHEELCHAIR?

The FDA product code for HI-RIDER WHEELCHAIR is IPL.

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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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