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FDA 510(k)

FEEL-DRCS

K-Number: K110033 · 2011-09-15

ApplicantImfou Co., Ltd.
Decision Date2011-09-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FEEL-DRCS is the device name listed in this FDA 510(k) record. The listed applicant is Imfou Co., Ltd.. It received FDA 510(k) clearance on 2011-09-15 under 510(k) number K110033. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEEL-DRCS?

FEEL-DRCS is a medical device that received FDA 510(k) clearance on 2011-09-15. The listed applicant is Imfou Co., Ltd.. The 510(k) number is K110033.

When did FEEL-DRCS receive FDA 510(k) clearance?

FEEL-DRCS received FDA 510(k) clearance on 2011-09-15, under 510(k) number K110033.

Who is the listed applicant for FEEL-DRCS?

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

What is the FDA product code for FEEL-DRCS?

The FDA product code for FEEL-DRCS is LLZ.

Related Devices (Code: LLZ)

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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