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FDA 510(k)

LEVO-STAND-UP WHEELCHAIR

K-Number: K790265 · 1979-02-13

Decision Date1979-02-13
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LEVO-STAND-UP WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Marion Laboratories, Inc.. It received FDA 510(k) clearance on 1979-02-13 under 510(k) number K790265. 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 LEVO-STAND-UP WHEELCHAIR?

LEVO-STAND-UP WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1979-02-13. The listed applicant is Marion Laboratories, Inc.. The 510(k) number is K790265.

When did LEVO-STAND-UP WHEELCHAIR receive FDA 510(k) clearance?

LEVO-STAND-UP WHEELCHAIR received FDA 510(k) clearance on 1979-02-13, under 510(k) number K790265.

Who is the listed applicant for LEVO-STAND-UP WHEELCHAIR?

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

What is the FDA product code for LEVO-STAND-UP WHEELCHAIR?

The FDA product code for LEVO-STAND-UP WHEELCHAIR is IPL.

Related Clinical Trials

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.

Other records listing Marion Laboratories, Inc. as applicant

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.

View all 38 devices →

Related Devices (Code: IPL)

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.

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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