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FDA 510(k)

KARMA POWER WHEELCHAIR, MODEL KP-25

K-Number: K041678 · 2004-07-23

Decision Date2004-07-23
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KARMA POWER WHEELCHAIR, MODEL KP-25 is the device name listed in this FDA 510(k) record. The listed applicant is Karma Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2004-07-23 under 510(k) number K041678. 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 KARMA POWER WHEELCHAIR, MODEL KP-25?

KARMA POWER WHEELCHAIR, MODEL KP-25 is a medical device that received FDA 510(k) clearance on 2004-07-23. The listed applicant is Karma Medical Products Co., Ltd.. The 510(k) number is K041678.

When did KARMA POWER WHEELCHAIR, MODEL KP-25 receive FDA 510(k) clearance?

KARMA POWER WHEELCHAIR, MODEL KP-25 received FDA 510(k) clearance on 2004-07-23, under 510(k) number K041678.

Who is the listed applicant for KARMA POWER WHEELCHAIR, MODEL KP-25?

The FDA 510(k) record lists Karma Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARMA POWER WHEELCHAIR, MODEL KP-25?

The FDA product code for KARMA POWER WHEELCHAIR, MODEL KP-25 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 Karma Medical Products Co., Ltd. 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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