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FDA 510(k)

LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800

K-Number: K050087 · 2005-02-01

Decision Date2005-02-01
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800 is the device name listed in this FDA 510(k) record. The listed applicant is Lerado Oversea Ltd. Twn Branch (Bvi). It received FDA 510(k) clearance on 2005-02-01 under 510(k) number K050087. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800?

LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800 is a medical device that received FDA 510(k) clearance on 2005-02-01. The listed applicant is Lerado Oversea Ltd. Twn Branch (Bvi). The 510(k) number is K050087.

When did LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800 receive FDA 510(k) clearance?

LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800 received FDA 510(k) clearance on 2005-02-01, under 510(k) number K050087.

Who is the listed applicant for LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800?

The FDA 510(k) record lists Lerado Oversea Ltd. Twn Branch (Bvi) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800?

The FDA product code for LERADO AVANTICARE POWER WHEELCHAIR, MODEL PW-1800 is ITI.

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 Lerado Oversea Ltd. Twn Branch (Bvi) 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.

Related Devices (Code: ITI)

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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