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FDA 510(k)

FORU KV10HB

K-Number: K072027 · 2007-08-20

ApplicantKwang Yang Motor Co., Ltd.
Decision Date2007-08-20
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORU KV10HB is the device name listed in this FDA 510(k) record. The listed applicant is Kwang Yang Motor Co., Ltd.. It received FDA 510(k) clearance on 2007-08-20 under 510(k) number K072027. 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 FORU KV10HB?

FORU KV10HB is a medical device that received FDA 510(k) clearance on 2007-08-20. The listed applicant is Kwang Yang Motor Co., Ltd.. The 510(k) number is K072027.

When did FORU KV10HB receive FDA 510(k) clearance?

FORU KV10HB received FDA 510(k) clearance on 2007-08-20, under 510(k) number K072027.

Who is the listed applicant for FORU KV10HB?

The FDA 510(k) record lists Kwang Yang Motor Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORU KV10HB?

The FDA product code for FORU KV10HB is ITI.

Other records listing Kwang Yang Motor 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.

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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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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