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FDA 510(k)

OLYMPUS AU 5000 FLAME PHOTOMETER MODULE

K-Number: K862148 · 1986-09-29

ApplicantOlympus Corp.
Decision Date1986-09-29
Product CodeJJO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

OLYMPUS AU 5000 FLAME PHOTOMETER MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1986-09-29 under 510(k) number K862148. The device is classified under product code JJO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS AU 5000 FLAME PHOTOMETER MODULE?

OLYMPUS AU 5000 FLAME PHOTOMETER MODULE is a medical device that received FDA 510(k) clearance on 1986-09-29. The listed applicant is Olympus Corp.. The 510(k) number is K862148.

When did OLYMPUS AU 5000 FLAME PHOTOMETER MODULE receive FDA 510(k) clearance?

OLYMPUS AU 5000 FLAME PHOTOMETER MODULE received FDA 510(k) clearance on 1986-09-29, under 510(k) number K862148.

Who is the listed applicant for OLYMPUS AU 5000 FLAME PHOTOMETER MODULE?

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

What is the FDA product code for OLYMPUS AU 5000 FLAME PHOTOMETER MODULE?

The FDA product code for OLYMPUS AU 5000 FLAME PHOTOMETER MODULE is JJO.

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.

Other records listing Olympus Corp. 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.

View all 142 devices →

Related Devices (Code: JJO)

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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