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FDA 510(k)

MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C

K-Number: K022446 · 2003-03-28

ApplicantAomori Olympus Co., Ltd.
Decision Date2003-03-28
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C is the device name listed in this FDA 510(k) record. The listed applicant is Aomori Olympus Co., Ltd.. It received FDA 510(k) clearance on 2003-03-28 under 510(k) number K022446. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C?

MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C is a medical device that received FDA 510(k) clearance on 2003-03-28. The listed applicant is Aomori Olympus Co., Ltd.. The 510(k) number is K022446.

When did MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C receive FDA 510(k) clearance?

MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C received FDA 510(k) clearance on 2003-03-28, under 510(k) number K022446.

Who is the listed applicant for MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C?

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

What is the FDA product code for MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C?

The FDA product code for MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C is EOQ.

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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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