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FDA 510(k)

LUMICO ANALYZER SA-300

K-Number: K923158 · 1992-11-17

Decision Date1992-11-17
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LUMICO ANALYZER SA-300 is the device name listed in this FDA 510(k) record. The listed applicant is Maruzen Petrochemical Co., Ltd.. It received FDA 510(k) clearance on 1992-11-17 under 510(k) number K923158. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUMICO ANALYZER SA-300?

LUMICO ANALYZER SA-300 is a medical device that received FDA 510(k) clearance on 1992-11-17. The listed applicant is Maruzen Petrochemical Co., Ltd.. The 510(k) number is K923158.

When did LUMICO ANALYZER SA-300 receive FDA 510(k) clearance?

LUMICO ANALYZER SA-300 received FDA 510(k) clearance on 1992-11-17, under 510(k) number K923158.

Who is the listed applicant for LUMICO ANALYZER SA-300?

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

What is the FDA product code for LUMICO ANALYZER SA-300?

The FDA product code for LUMICO ANALYZER SA-300 is JJQ.

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.

Related Devices (Code: JJQ)

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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