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FDA 510(k)

MICROLITE WHEELCHAIR

K-Number: K933919 · 1993-09-30

ApplicantMorgan Technology, Inc.
Decision Date1993-09-30
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MICROLITE WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Morgan Technology, Inc.. It received FDA 510(k) clearance on 1993-09-30 under 510(k) number K933919. 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 MICROLITE WHEELCHAIR?

MICROLITE WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1993-09-30. The listed applicant is Morgan Technology, Inc.. The 510(k) number is K933919.

When did MICROLITE WHEELCHAIR receive FDA 510(k) clearance?

MICROLITE WHEELCHAIR received FDA 510(k) clearance on 1993-09-30, under 510(k) number K933919.

Who is the listed applicant for MICROLITE WHEELCHAIR?

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

What is the FDA product code for MICROLITE WHEELCHAIR?

The FDA product code for MICROLITE 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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