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FDA 510(k)

RAPIDIACOLON

K-Number: K041761 · 2004-07-13

ApplicantInfinitt Co., Ltd.
Decision Date2004-07-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RAPIDIACOLON is the device name listed in this FDA 510(k) record. The listed applicant is Infinitt Co., Ltd.. It received FDA 510(k) clearance on 2004-07-13 under 510(k) number K041761. 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 RAPIDIACOLON?

RAPIDIACOLON is a medical device that received FDA 510(k) clearance on 2004-07-13. The listed applicant is Infinitt Co., Ltd.. The 510(k) number is K041761.

When did RAPIDIACOLON receive FDA 510(k) clearance?

RAPIDIACOLON received FDA 510(k) clearance on 2004-07-13, under 510(k) number K041761.

Who is the listed applicant for RAPIDIACOLON?

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

What is the FDA product code for RAPIDIACOLON?

The FDA product code for RAPIDIACOLON is LLZ.

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Other records listing Infinitt 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: LLZ)

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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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